[{"last_updated":1780506228,"legal":"API Terms of Service: Please link back (with follow, and without nofollow!) to the URL on Remote OK and mention Remote OK as a source, so we get traffic back from your site. If you do not we'll have to suspend API access.\n\nPlease don't use the Remote OK logo without written permission as it's a registered trademark, please DO use our name Remote OK though."},{"slug":"remote-gerente-de-cuentas-madrid-espana-andalucia-espana-valenci-sixtema-1132754","id":"1132754","epoch":1780422106,"date":"2026-06-02T17:41:46+00:00","company":"Sixtema","company_logo":"","position":"Gerente De Cuentas Madrid Espa\u00c3\u00b1a ; Andaluc\u00c3\u00ada Espa\u00c3\u00b1a; Valenci ..","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time","english teacher","teaching","testing","mobile","marketing"],"description":"Gerente de Cuentas (Key Account Manager) (Remoto)<br><br>Si te apasiona la tecnolog\u00c3\u00ada y la innovaci\u00c3\u00b3n, y quieres desarrollarte profesionalmente en un proyecto estable y con proyecci\u00c3\u00b3n en el sector TIC, tu sitio est\u00c3\u00a1 en SIXTEMA.<br><br>Seguimos buscando talento, por lo que queremos ampliar nuestro equipo operativo con un perfil con experiencia como Gerente de cuentas.<br><br>Descripci\u00c3\u00b3n de la oferta<br><br>Si te apasiona la tecnolog\u00c3\u00ada y la innovaci\u00c3\u00b3n, y quieres desarrollarte profesionalmente en un proyecto estable y con proyecci\u00c3\u00b3n en el sector TIC, tu sitio est\u00c3\u00a1 en SIXTEMA.<br><br>Seguimos buscando talento, por lo que queremos ampliar nuestro equipo operativo con un perfil con experiencia como Gerente de cuentas.<br><br>Rol<br><br>Gerente de Cuentas (Key Account Manager) (Remoto)<br><br>Formaci\u00c3\u00b3n Requerida<br><br>Formaci\u00c3\u00b3n universitaria en Administraci\u00c3\u00b3n y Direcci\u00c3\u00b3n de Empresas, Marketing, Ingenier\u00c3\u00ada Inform\u00c3\u00a1tica o afines.<br><br>Requisitos Imprescindibles<br><br>Experiencia m\u00c3\u00adnima de 4 a\u00c3\u00b1os en la venta de proyectos de IT complejos a los clientes del sector p\u00c3\u00bablico y privado.<br><br>Acostumbrado\/a a tratar con diferentes niveles de interlocuci\u00c3\u00b3n, tanto en IT, como en compras y las \u00c3\u00a1reas de negocio.<br><br>Capacidad de influencia, generaci\u00c3\u00b3n de demanda, perfil de venta consultiva e generador de confianza en sus clientes.<br><br>Capacidad de establecer relaciones a largo plazo.<br><br>Experiencia demostrable en venta consultiva y desarrollo de negocio, incluido el Sector P\u00c3\u00bablico.<br><br>S\u00c3\u00b3lidas habilidades de comunicaci\u00c3\u00b3n, negociaci\u00c3\u00b3n y cierre.<br><br>Perfil aut\u00c3\u00b3nomo, proactivo y orientado a resultados.<br><br>Conocimiento de soluciones tecnol\u00c3\u00b3gicas y servicios IT.<br><br>Requisitos Valorables<br><br>Conocimientos espec\u00c3\u00adficos del Sector P\u00c3\u00bablico.<br><br>Formaci\u00c3\u00b3n adicional en t\u00c3\u00a9cnicas de venta.<br><br>Experiencia previa comercializando soluciones de gesti\u00c3\u00b3n para Administraciones P\u00c3\u00bablicas.<br><br>Funciones Principales<br><br>Identificar, prospectar y desarrollar nuevas oportunidades de negocio en el \u00c3\u00a1mbito designado.<br><br>Gestionar de principio a fin el ciclo comercial de nuestras soluciones: prospecci\u00c3\u00b3n, an\u00c3\u00a1lisis consultivo, presentaci\u00c3\u00b3n de propuestas, negociaci\u00c3\u00b3n y cierre.<br><br>Realizar presentaciones, demos funcionales, visitas y seguimiento activo de las ofertas.<br><br>Detectar necesidades dentro de la base instalada y potenciar el cross-selling del portfolio de Sixtema.<br><br>Acompa\u00c3\u00b1ar, asesorar y guiar a clientes y potenciales clientes durante todo el proceso.<br><br>Mantenerte al d\u00c3\u00ada de nuestras soluciones, de la competencia y de las tendencias del sector p\u00c3\u00bablico.<br><br>Gestionar tu pipeline, previsiones y actividad diaria en CRM y herramientas colaborativas.<br><br>Participar en licitaciones y procesos administrativos conforme a nuestros procedimientos internos.<br><br>\u00c2\u00bfQu\u00c3\u00a9 te ofrecemos?<br><br>Unirte a una empresa en crecimiento y con proyecci\u00c3\u00b3n.<br><br>Participar en proyectos innovadores y con tecnolog\u00c3\u00adas en auge.<br><br>Formar parte de un equipo de profesionales con enfoque en mejora continua y calidad.<br><br>Estabilidad y desarrollo profesional.<br><br>Medidas de conciliaci\u00c3\u00b3n mediante horario flexible, trabajo remoto, y jornada intensiva todos los viernes y los meses de julio y agosto.<br><br>Retribuci\u00c3\u00b3n flexible: seguro m\u00c3\u00a9dico.<br><br>Buen ambiente de trabajo.<br><br>23 d\u00c3\u00adas de vacaciones, adem\u00c3\u00a1s del 24 y 31 de diciembre.<br><br>Plan referido, asociado a una compensaci\u00c3\u00b3n si nos recomiendas a un amigo\/a.<br><br>Plan de formaci\u00c3\u00b3n, formaci\u00c3\u00b3n continua en modalidades en directo y con plataformas.<br><br>Participaci\u00c3\u00b3n en actividades de equipo.<br><br>Cultura inclusiva y diversidad: cada persona tiene algo que aportar; toda idea es importante.<br><br>Si te identificas, \u00c3\u00banete al equipo.<br><br>Env\u00c3\u00ada tu CV a ******<br><br>#J-*****-Ljbffr<br\/><br\/>Please mention the word **IMPROVED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Oria, ","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-gerente-de-cuentas-madrid-espana-andalucia-espana-valenci-sixtema-1132754","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-gerente-de-cuentas-madrid-espana-andalucia-espana-valenci-sixtema-1132754"},{"slug":"remote-creative-designer-air-apps-1132755","id":"1132755","epoch":1780409235,"date":"2026-06-02T14:07:15+00:00","company":"Air Apps","company_logo":"","position":"Creative Designer","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time","english teacher","teaching","testing","mobile","marketing","design","designer","web dev","finance","ads","content writing","photoshop","medical","illustrator"],"description":"<strong>About Air Apps<br><br><\/strong>At Air Apps, we believe in thinking bigger\u00e2\u0080\u0094and moving faster. We\u00e2\u0080\u0099re a family-founded company on a mission to create the world\u00e2\u0080\u0099s first AI-powered Personal &amp; Entrepreneurial Resource Planner (PRP), and we need your passion and ambition to help us change how people plan, work, and live. Born in Lisbon, Portugal in 2018\u00e2\u0080\u0094and now with offices in both Lisbon and San Francisco\u00e2\u0080\u0094we\u00e2\u0080\u0099ve remained self-funded while reaching over 100 million downloads worldwide.<br><br>Our long-term focus drives us to challenge the status quo every day, pushing the boundaries of AI-driven solutions that truly make a difference. Here, you\u00e2\u0080\u0099ll be a creative force, shaping products that empower people across the globe.<br><br>Join us on this journey to redefine resource management\u00e2\u0080\u0094and change lives along the way.<br><br><strong>The Role<br><br><\/strong>As a Creative Designer at Air Apps, you will play a crucial role in shaping our brand identity and delivering visually engaging designs across multiple platforms. You will collaborate with various teams to ensure a cohesive and compelling user experience, working on digital ads, social media content, landing pages, email campaigns, and print materials.<br><br><ul><li>This is a fully onsite position, based at our office in Lisbon, where you will collaborate closely with cross-functional teams in person and contribute to a dynamic and fast-paced environment. We are open to support with relocation efforts. <br><br><\/li><\/ul><strong>Responsibilities<br><br><\/strong><ul><li>Develop and maintain a consistent visual identity that aligns with Air Apps\u00e2\u0080\u0099 brand guidelines. <\/li><li>Create engaging graphics, illustrations, infographics, and layouts for web, social media, email campaigns, and print materials. <\/li><li>Collaborate with Marketing, Product, and Content teams to translate requirements into compelling visual solutions. <\/li><li>Iterate on designs based on feedback from stakeholders and refine assets using user insights and performance metrics. <\/li><li>Ensure high-quality output and conduct design quality assurance across various channels. <\/li><li>Utilize industry-standard design software (e.g., Adobe Creative Suite, Figma) to create and deliver assets in multiple formats. <br><br><\/li><\/ul><strong>Requirements<br><br><\/strong><ul><li>Bachelor's degree in Graphic Design, Fine Arts, or a related field. <\/li><li>Around 3 years of experience creating assets for digital marketing campaigns, social media, and web. <\/li><li>Strong portfolio showcasing a range of design projects and styles. <\/li><li>Knowledge of typography, color theory, layout, and design best practices. <\/li><li>Proficiency in industry-standard design tools such as Adobe Creative Suite (Photoshop, Illustrator, InDesign) and Figma. <\/li><li>Strong communication, time-management, and attention-to-detail skills. <\/li><li>Ability to work in a fast-paced, remote environment and collaborate effectively across teams. <br><br><\/li><\/ul><strong>What benefits are we offering?<br><br><\/strong><ul><li>Apple hardware ecosystem for work. <\/li><li>Annual Bonus<\/li><li>Top-tier Health and Life Insurance for peace of mind. <\/li><li>Transportation Budget to support your commute needs. <\/li><li>Coverflex benefits package for meal allowances, well-being, and more. <\/li><li>Childcare support. <\/li><li>Air Conference - an opportunity to meet the team, collaborate, and grow together. <\/li><li>Pension Fund to support your long-term financial planning. <\/li><li>Urban Sports Club membership to keep you active. <\/li><li>Meals 100% free at the hub. <br><br><\/li><\/ul><strong>Diversity &amp; Inclusion<br><br><\/strong>At Air Apps, we are committed to fostering a diverse, inclusive, and equitable workplace. We enthusiastically welcome applicants from all backgrounds, experiences, and perspectives. We celebrate diversity in all its forms and believe that varied voices and experiences make us stronger.<br><br><strong>Application Disclaimer<br><br><\/strong>At Air Apps, we value transparency and integrity in our hiring process. Applicants must submit their own work without any AI-generated assistance. Any use of AI in application materials, assessments, or interviews will result in disqualification.<br><br>Compensation Range: \u00e2\u0082\u00ac44K - \u00e2\u0082\u00ac55K<br><br><br\/><br\/>Please mention the word **EXCEEDS** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Z\u00c3\u00bcrich, Z\u00c3\u00bcrich, Z\u00c3\u00bcrich, Schweiz","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-creative-designer-air-apps-1132755","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-creative-designer-air-apps-1132755"},{"slug":"remote-project-assistant-arabian-private-holdings-1132749","id":"1132749","epoch":1780409035,"date":"2026-06-02T14:03:55+00:00","company":"Arabian Private Holdings","company_logo":"","position":"Project Assistant","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time"],"description":"<strong>Employment setup<br><\/strong> <p> This is a full-time, permanent position operated on a remote basis. Arabian Private Holdings is a Saudi Arabian firm, and this role is conducted as a remote engagement. Candidates should be based in Bulgaria or within a neighboring region to ensure manageable timezone overlap. You must already possess the legal right to work in your current country of residence. While the firm is headquartered in Riyadh, the day to day work for this role involves direct support for a specific project involving an international logistics firm with active operations in Bulgaria. We require a minimum of five hours overlap with the Saudi Arabia workday (UTC+3). This role is paid and includes professional development through direct work with the firm principals. The hiring process involves an initial review of written materials, a logical reasoning assessment, and two rounds of video interviews. <\/p>  <br><strong>About the role<br><\/strong> <p> The Project Assistant provides the organizational backbone for our client mandates, ensuring that administrative tasks do not hinder the progress of our strategic work. This position exists to manage the flow of information between the principals and our clients, specifically as we coordinate a governance review for an international logistics firm. It is a necessary function that allows our senior partners to stay focused on high level analysis while you maintain the structured documentation required for successful project delivery. <\/p>  <br><strong>About Arabian Private Holdings<br><\/strong> <p> Arabian Private Holdings operates on the principle that many corporate problems are solved through direct attention rather than large teams of junior staff. We work with family groups, listed corporations, and government entities to provide honest, independent advice on strategy and portfolio Management. Our structure is principal led: every client receives the direct focus of the people accountable for the results. We avoid complex hierarchies and focus on providing a clear view of business performance. We are a remote firm, choosing to prioritize the quality of our thought and the strength of our relationships over physical office presence. <\/p>  <br><strong>What you will do<\/strong><ul> <li>Maintain and update project schedules to track the completion of specific milestones for our logistics sector clients.<\/li> <li>Coordinate meetings and prepare briefing notes that summarize the key points discussed during partner sessions.<\/li> <li>Conduct basic desk research on industry trends and regulatory changes within the logistics and transport sectors.<\/li> <li>Draft initial versions of project reports, ensuring that the grammar and formatting meet the firm standards.<\/li> <li>Keep our internal document folders organized so that all versions of a mandate are easily accessible to the principals.<\/li> <li>Follow up on information requests sent to client teams to ensure data is received on time for our weekly reviews.<\/li> <li>Monitor specific project emails and flag urgent requests that require immediate principal attention.<\/li> <li>Prepare presentation slides based on handwritten notes or rough drafts provided by the partners.<\/li> <br><br><\/ul><strong>What we are looking for<\/strong><ul> <li>A high degree of written precision and the ability to summarize complex information into simple sentences.<\/li> <li>Comfortable using standard office tools such as Microsoft Word, Excel, and shared document platforms.<\/li> <li>Logical rigor in organizing tasks and a preference for order and structure in your daily work.<\/li> <li>Eager to learn about corporate governance and how large holding companies operate.<\/li> <li>Familiar with the basic concepts of project coordination and managing deadlines.<\/li> <li>Able to work independently in a remote environment while keeping the team updated on progress.<\/li> <li>Some exposure to business environments through internships or previous entry level office roles.<\/li> <br><br><\/ul><strong>How we work<br><\/strong> <p> We operate as a lean, remote team that values quiet productivity and direct communication. Our way of working is built on trust and the assumption that everyone is capable of managing their own schedule to meet deadlines. We do not believe in unnecessary meetings or long email threads: we prefer brief, clear updates. Because we are a principal led firm, you will have regular interactions with senior partners who will provide guidance on your work. We focus on getting the work right the first time and take pride in the accuracy of our documentation. This role offers an environment where your contributions have a visible effect on the outcome of a mandate. <\/p>  <br><strong>What the role offers<\/strong><ul> <li>Broad exposure to the decision making processes of major international holding companies.<\/li> <li>Flexible remote working that allows you to manage your time without a commute.<\/li> <li>Direct mentoring from experienced partners who are leaders in their respective fields.<\/li> <li>Training in professional writing and the development of structured logical thinking.<\/li> <li>The opportunity to support a high priority project for an international logistics client.<\/li> <li>A stable, full time position within a professional firm that values quality over volume.<\/li><\/ul><br\/><br\/>Please mention the word **CHERISH** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Sofia, Sofia, Sofia City, Bulgaria","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-project-assistant-arabian-private-holdings-1132749","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-project-assistant-arabian-private-holdings-1132749"},{"slug":"remote-english-teacher-for-children-tus-media-1132750","id":"1132750","epoch":1780396510,"date":"2026-06-02T10:35:10+00:00","company":"TUS Media","company_logo":"","position":"English Teacher for Children","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time","english teacher","teaching"],"description":"At <strong>Tusclasesparticulares<\/strong>, we are looking for <strong>English teachers specialized in children<\/strong> to join our team immediately and give private lessons online or in person.<br><br>The demand for English tutoring for young learners continues to grow, and we are seeking motivated individuals with a good command of English and a passion for teaching children in an engaging and dynamic way.<br><br><strong>\u00f0\u009f\u008e\u00af Requirements<br><br><\/strong><ul><li> Good level of English (B2\u00e2\u0080\u0093C1 recommended or higher).<\/li><li> Enjoy working with children and teaching in a fun, interactive way.<\/li><li> Previous teaching experience is a plus, but not required.<br><br><\/li><\/ul><strong>\u00f0\u009f\u0092\u00bc What We Offer<br><br><\/strong><ul><li> Flexible schedule (you choose your availability).<\/li><li> Online, in-person, or hybrid classes.<\/li><li> No minimum working hours required.<\/li><li> Pay between \u00e2\u0082\u00ac15 and \u00e2\u0082\u00ac30 per hour.<br><br><\/li><\/ul>A great opportunity for students, teachers, or English speakers looking for a flexible side income while helping children learn and grow.<br><br>\u00f0\u009f\u0091\u0089 Apply now and start teaching whenever you want<br\/><br\/>Please mention the word **FAV** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Hospitalet de Llobregat, Hospitalet de Llobregat, Catalu\u00c3\u00b1a, Espa\u00c3\u00b1a","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-english-teacher-for-children-tus-media-1132750","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-english-teacher-for-children-tus-media-1132750"},{"slug":"remote-british-english-voice-actor-specialist-lancaster-opsarmy-careers-1132748","id":"1132748","epoch":1780366763,"date":"2026-06-02T02:19:23+00:00","company":"OpsArmy Careers","company_logo":"","position":"British English Voice Actor Specialist Lancaster","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad"],"description":"<strong><strong>British English Voice Actor Specialist<br><br><\/strong><\/strong><em><strong><strong>Qualified applicants will be contacted via email regarding the next steps in the hiring process<br><br><\/strong><\/strong><\/em>We are seeking a talented and versatile British English Voice Actor Specialist to support AI and machine learning projects by delivering high-quality voice recordings across various scripts, tones, and speaking styles. The ideal candidate has strong vocal control, excellent pronunciation, and the ability to perform naturally while following detailed project requirements.<br><br><strong>Responsibilities<br><br><\/strong><ul><li>Record voice scripts with clear pronunciation, natural delivery, and appropriate tone<\/li><li>Perform a variety of speaking styles, emotions, and character voices as required by the project<\/li><li>Follow recording guidelines, pronunciation standards, and script instructions<\/li><li>Deliver high-quality audio recordings free from background noise and technical issues<\/li><li>Review recordings for accuracy, consistency, and completeness before submission<\/li><li>Meet project deadlines and recording targets<\/li><li>Communicate any script ambiguities, technical issues, or recording challenges to the project team<\/li><li>Maintain professionalism and consistency across all recordings<br><br><br><\/li><\/ul><strong>Requirements<br><br><\/strong><ul><li>Native or near-native proficiency in British English<\/li><li>Excellent vocal clarity, articulation, and pronunciation<\/li><li>Ability to adapt tone, pace, emotion, and speaking style based on project needs<\/li><li>Strong reading comprehension and script interpretation skills<\/li><li>Reliable internet connection and access to a quiet recording environment<\/li><li>Basic computer skills and ability to use online recording platforms<\/li><li>Ability to work independently and follow detailed instructions<br><br><br><\/li><\/ul>Nice to Have<br><br><ul><li>Previous experience in voice acting, voice-over, podcasting, broadcasting, or related audio work<\/li><li>Experience recording for AI, speech recognition, audiobook, gaming, or media projects<\/li><li>Familiarity with audio recording software and editing tools<\/li><li>Access to professional recording equipment, including a quality microphone and sound-treated recording space<br><br><br><\/li><\/ul><em><strong><strong>Qualified applicants will be contacted via email regarding the next steps in the hiring process<\/strong><\/strong><\/em><br\/><br\/>Please mention the word **GORGEOUSLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Lancashire, Lancashire, England, United Kingdom","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-british-english-voice-actor-specialist-lancaster-opsarmy-careers-1132748","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-british-english-voice-actor-specialist-lancaster-opsarmy-careers-1132748"},{"slug":"remote-copywriter-yo-it-consulting-1132757","id":"1132757","epoch":1780364831,"date":"2026-06-02T01:47:11+00:00","company":"YO IT Consulting","company_logo":"","position":"Copywriter","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time","english teacher","teaching","testing","mobile","marketing","design","designer","web dev","finance","ads","content writing","photoshop","medical","illustrator","consulting","copywriting","quality assurance","sys admin","part time"],"description":"<strong>Job Type:<\/strong> Contract, Part-time<br><br><strong>Location:<\/strong> Remote<br><br>Role Description<br><br>In this hourly, remote contractor role, you will work as a Copywriting &amp; Content Subject Matter Expert (SME) to review AI-generated marketing\/content-writing outputs and\/or create expert copy and content, evaluating reasoning quality, intent alignment, and step-by-step writing decisions while providing precise written feedback. You will assess solutions for accuracy, clarity, brand fit, tone, and adherence to the prompt; identify issues in logic, messaging, audience targeting, claims\/compliance risk, structure, and style; fact-check statements where needed; write high-quality explanations and model outputs that demonstrate strong copywriting technique; and rate and compare multiple responses based on effectiveness, correctness, and reasoning quality. This role is with a fast-growing AI Data Services company delivering training data for many of the world\u00e2\u0080\u0099s largest AI companies and foundation-model labs. Your copywriting expertise directly helps improve the world\u00e2\u0080\u0099s premier AI models by making their writing more persuasive, accurate, on-brand, and clearly explained. Important: There is no immediate project for this role; however, if qualified, you will be among the first experts we reach out to when relevant opportunities arise. This will also provide you with access to future projects available through our expert network.<br><br><strong>Your Profile<br><br><\/strong><ul><li>Bachelor\u00e2\u0080\u0099s degree (or higher) in Communications, Marketing, Journalism, English, or a related field (or equivalent professional experience). <\/li><li>5+ years of professional experience in copywriting, content writing, editorial, content marketing, or brand storytelling. <\/li><li>Strong command of brand voice, tone adaptation, and audience-aware writing (B2B and\/or B2C). <\/li><li>Ability to evaluate and improve writing for clarity, structure, persuasion, and consistency, including headlines, CTAs, and narrative flow. <\/li><li>Demonstrated ability to spot and correct factual errors, weak reasoning, overclaims, and potential compliance issues (especially in regulated domains). <\/li><li>Familiarity with common content formats: landing pages, email campaigns, blog posts, ads, social posts, product copy, scripts, and long-form guides. <\/li><li>Comfort providing specific, actionable feedback and writing gold-standard rewrites with rationale; minimum C1 English proficiency. <\/li><li>Reliable, self-directed, and able to deliver consistent quality in an hourly, remote contractor workflow across time zones. <\/li><li>Prior experience with AI data training\/annotation, content QA, editorial operations, or style-guide governance is strongly preferred. <br><br><\/li><\/ul><strong>Key Responsibilities<br><br><\/strong><ul><li>Develop AI Training Content: Create detailed prompts and gold-standard copy\/content across multiple formats and industries to guide AI learning. <\/li><li>Optimize AI Performance: Evaluate and rank AI responses to improve clarity, persuasion, tone match, and factual reliability. <\/li><li>Ensure Model Integrity: Test AI outputs for inaccuracies, hallucinated claims, bias, unsafe advice, and brand-risk issues; validate reliability across use cases.<\/li><\/ul><br\/><br\/>Please mention the word **LAVISH** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Manchester, Manchester, England, United Kingdom","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-copywriter-yo-it-consulting-1132757","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-copywriter-yo-it-consulting-1132757"},{"slug":"remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132753","id":"1132753","epoch":1780333885,"date":"2026-06-01T17:11:25+00:00","company":"Jobster","company_logo":"","position":"Game Tester &amp; Survey Taker Immediate Start Freecash","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time","english teacher","teaching","testing","mobile"],"description":"Are you looking for a flexible work from home opportunity? On Freecash, you are in control of your earnings. We provide a platform where you can choose from a wide range of paid online tasks, including testing mobile games, participating in market research, and completing digital offers.<br><br>There are no shifts, no contracts, and no fixed schedules. You simply log in whenever you want, from anywhere in the UK, and earn rewards for every task you complete. This is the perfect role for students, stay-at-home parents, or anyone looking for a side hustle.<br><br><strong>What You Will Be Doing<br><br><\/strong>You will choose tasks that fit your interests and schedule. Typical activities include:<br><br><br><ul><li>Game Testing: Playing mobile games to reach a specific level.<\/li><li>Market Research: Answering online surveys and sharing your opinions on products.<\/li><li>Digital Tasks: Completing trial or promotional offers from our partners.<\/li><li>Earning: Accumulating coins for every completed activity, which can be exchanged for real cash (PayPal) or gift cards.<br><br><br><\/li><\/ul><strong>What We Offer<br><br><br><\/strong><ul><li>Remote Work: Work from anywhere with an internet connection.<\/li><li>Total Flexibility: You decide when and how often you participate.<\/li><li>Immediate Start: No interview process\u00e2\u0080\u0094start earning immediately.<\/li><li>Sign-up Bonus: Get a $5 bonus automatically once you complete your first offer.<\/li><li>Fast Payouts: Exchange your earned coins for cash and gift cards easily.<br><br><br><\/li><\/ul><strong>Requirements<br><br><br><\/strong><ul><li>No Experience Needed: No minimum education is required.<\/li><li>Tech: Access to a computer or smartphone with a stable internet connection.<\/li><li>Mindset: Willingness to complete tasks carefully and accurately.<br><br><br><\/li><\/ul><strong>Ready to start earning?<br><br><\/strong>Click Apply Now to create your Freecash account. Your $5 bonus will be added automatically as soon as you begin your first offer.<br><br>#Jobster<br\/><br\/>Please mention the word **ENTERTAINING** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Blackpool, Blackpool, England, United Kingdom","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132753","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132753"},{"slug":"remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132752","id":"1132752","epoch":1780333884,"date":"2026-06-01T17:11:24+00:00","company":"Jobster","company_logo":"","position":"Game Tester &amp; Survey Taker Immediate Start Freecash","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time","english teacher","teaching","testing","mobile"],"description":"Are you looking for a flexible work from home opportunity? On Freecash, you are in control of your earnings. We provide a platform where you can choose from a wide range of paid online tasks, including testing mobile games, participating in market research, and completing digital offers.<br><br>There are no shifts, no contracts, and no fixed schedules. You simply log in whenever you want, from anywhere in the UK, and earn rewards for every task you complete. This is the perfect role for students, stay-at-home parents, or anyone looking for a side hustle.<br><br><strong>What You Will Be Doing<br><br><\/strong>You will choose tasks that fit your interests and schedule. Typical activities include:<br><br><br><ul><li>Game Testing: Playing mobile games to reach a specific level.<\/li><li>Market Research: Answering online surveys and sharing your opinions on products.<\/li><li>Digital Tasks: Completing trial or promotional offers from our partners.<\/li><li>Earning: Accumulating coins for every completed activity, which can be exchanged for real cash (PayPal) or gift cards.<br><br><br><\/li><\/ul><strong>What We Offer<br><br><br><\/strong><ul><li>Remote Work: Work from anywhere with an internet connection.<\/li><li>Total Flexibility: You decide when and how often you participate.<\/li><li>Immediate Start: No interview process\u00e2\u0080\u0094start earning immediately.<\/li><li>Sign-up Bonus: Get a $5 bonus automatically once you complete your first offer.<\/li><li>Fast Payouts: Exchange your earned coins for cash and gift cards easily.<br><br><br><\/li><\/ul><strong>Requirements<br><br><br><\/strong><ul><li>No Experience Needed: No minimum education is required.<\/li><li>Tech: Access to a computer or smartphone with a stable internet connection.<\/li><li>Mindset: Willingness to complete tasks carefully and accurately.<br><br><br><\/li><\/ul><strong>Ready to start earning?<br><br><\/strong>Click Apply Now to create your Freecash account. Your $5 bonus will be added automatically as soon as you begin your first offer.<br><br>#Jobster<br\/><br\/>Please mention the word **CALMNESS** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Reading, Reading, England, United Kingdom","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132752","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132752"},{"slug":"remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132756","id":"1132756","epoch":1780333710,"date":"2026-06-01T17:08:30+00:00","company":"Jobster","company_logo":"","position":"Game Tester &amp; Survey Taker Immediate Start Freecash","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time","english teacher","teaching","testing","mobile","marketing","design","designer","web dev","finance","ads","content writing","photoshop","medical","illustrator"],"description":"Are you looking for a flexible work from home opportunity? On Freecash, you are in control of your earnings. We provide a platform where you can choose from a wide range of paid online tasks, including testing mobile games, participating in market research, and completing digital offers.<br><br>There are no shifts, no contracts, and no fixed schedules. You simply log in whenever you want, from anywhere in the UK, and earn rewards for every task you complete. This is the perfect role for students, stay-at-home parents, or anyone looking for a side hustle.<br><br><strong>What You Will Be Doing<br><br><\/strong>You will choose tasks that fit your interests and schedule. Typical activities include:<br><br><br><ul><li>Game Testing: Playing mobile games to reach a specific level.<\/li><li>Market Research: Answering online surveys and sharing your opinions on products.<\/li><li>Digital Tasks: Completing trial or promotional offers from our partners.<\/li><li>Earning: Accumulating coins for every completed activity, which can be exchanged for real cash (PayPal) or gift cards.<br><br><br><\/li><\/ul><strong>What We Offer<br><br><br><\/strong><ul><li>Remote Work: Work from anywhere with an internet connection.<\/li><li>Total Flexibility: You decide when and how often you participate.<\/li><li>Immediate Start: No interview process\u00e2\u0080\u0094start earning immediately.<\/li><li>Sign-up Bonus: Get a $5 bonus automatically once you complete your first offer.<\/li><li>Fast Payouts: Exchange your earned coins for cash and gift cards easily.<br><br><br><\/li><\/ul><strong>Requirements<br><br><br><\/strong><ul><li>No Experience Needed: No minimum education is required.<\/li><li>Tech: Access to a computer or smartphone with a stable internet connection.<\/li><li>Mindset: Willingness to complete tasks carefully and accurately.<br><br><br><\/li><\/ul><strong>Ready to start earning?<br><br><\/strong>Click Apply Now to create your Freecash account. Your $5 bonus will be added automatically as soon as you begin your first offer.<br><br>#Jobster<br\/><br\/>Please mention the word **RECOMMENDED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Luton, Luton, England, United Kingdom","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132756","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-game-tester-amp-survey-taker-immediate-start-freecash-jobster-1132756"},{"slug":"remote-abogada-grafton-1132751","id":"1132751","epoch":1780162900,"date":"2026-05-30T17:41:40+00:00","company":"Grafton","company_logo":"","position":"Abogada","tags":["biotech","speech","game dev","technical","customer support","dev","digital nomad","virtual assistant","education","video","microsoft","exec","senior","junior","ops","excel","legal","full time","english teacher","teaching"],"description":"Desde el departamento de Tax and Legal de Grafton estamos en la b\u00c3\u00basqueda de un Abogado Procesalista Senior para incorporarse a firma nacional de abogados,ubicada en Madrid.Funciones:Direcci\u00c3\u00b3n y estrategia procesal en procedimientos judiciales complejos.Gesti\u00c3\u00b3n integral de asuntos de litigaci\u00c3\u00b3n compleja civil y mercantil.Participaci\u00c3\u00b3n activa en procedimientos de arbitraje nacional e internacional.Coordinaci\u00c3\u00b3n y supervisi\u00c3\u00b3n de abogados junior y equipo a cargo.Interlocuci\u00c3\u00b3n directa con clientes nacionales e internacionales.Asistencia a reuniones comerciales y de seguimiento con clientes.Desarrollo de negocio y detecci\u00c3\u00b3n de oportunidades comerciales.Requisitos:Grado en Derecho y M\u00c3\u00a1ster de Acceso a la Abogac\u00c3\u00ada.Experiencia previa en despachos de abogados, de m\u00c3\u00adnimo 6 a\u00c3\u00b1os.Conocimientos y experiencia acreditable en arbitraje nacional e internacional.Capacidad de liderazgo y experiencia gestionando equipos.Nivel Avanzado de ingl\u00c3\u00a9s.Capacidad para trabajar con alto nivel de detalle y bajo presi\u00c3\u00b3n.Perfil con orientaci\u00c3\u00b3n a negocio y capacidad para generar confianza y oportunidades.Soft skills; Persona proactiva orientada al detalle, con excelentes habilidades de comunicaci\u00c3\u00b3n y capacidad para tomar decisiones, acostumbrada a ritmos altos y deadlines ajustados.Si te interesa un cambio, por favor inscr\u00c3\u00adbete o remite tu CV a ******\u00c2\u00a1Muchas gracias!<br\/><br\/>Please mention the word **QUALIFY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Valladolid, ","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-abogada-grafton-1132751","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-abogada-grafton-1132751"},{"slug":"remote-civil-service-secretary-chief-examiner-city-of-pullman-1132560","id":"1132560","epoch":1780041200,"date":"2026-05-29T07:53:20+00:00","company":"City of Pullman","company_logo":"","position":"Civil Service Secretary Chief Examiner","tags":["hr","consulting","coordinator","customer support","marketing","payroll","exec","biotech","medical","sys admin","php","recruiter"],"description":"<strong>Description<br><br><\/strong>The City of Pullman Civil Service Commission is currently recruiting for an independent contractor for the Secretary and Chief Examiner. The salary range position is $400.00-$600.00 monthly.<br><br>The Civil Service Commission Secretary and Chief Examiner performs all responsible supervisory and professional functions necessary for the administration and direction of the City Civil Service Commission in accordance with the Civil Service Rules and Regulations and provisions of state law relating to civil service. Acts independently. This position reports to and takes direction from the Civil Service Commission.<br><br><strong>Minimum Qualifications<br><br><\/strong><ul><li>AA or BA in business, psychology, social sciences, paralegal, human resources, or a related field, or three years of relevant experience.<\/li><li>The secretary and chief examiner shall be a properly qualified citizen of the city.<br><br><\/li><\/ul><strong>Essential Duties And Responsibilities<br><br><\/strong><ul><li>Evaluates and\/or supervises the evaluation of applicants meeting the minimum qualifications; determines which examinations will be conducted, the subjects to be covered in each examination, and the relative weights to be given to each portion of the examination, subject to approval of the Commission.<\/li><li>Supervises the conduct of all examination(s), appointing such experts, special examiners, or proctors as needed.<\/li><li>In coordination with the appropriate Police or Fire Chief, decides all questions relating to the eligibility of applicants, the admissibility of applicants to the examinations, extension of time, and all questions arising during an examination.<\/li><li>Recommends certification of successful candidates to the appropriate eligibility list, subject to approval of the Commission.<\/li><li>Performs all other functions necessary for the proper carrying out of these rules and provisions of law relating to the Civil Service System, and such additional duties as may be assigned from time to time by the Commission.<\/li><li>Attends all Commission meetings and records the votes taken, causes the minutes to be prepared and presented, refers proposed minimum qualifications and other examination related matters to the Commission for consideration and approval.<\/li><li>Uses technology systems to communicate with others and to perform and manage work.<\/li><li>Works an unpredictable schedule that may include up to eight hours or more in a single day.<\/li><li>Meets deadlines regardless of time pressure and stressful circumstances.<br><br><\/li><\/ul>Follows the Commission\u00e2\u0080\u0099s specific directives. Maintains reliable and regular attendance and is readily available to the Commission, police, fire, and other city officials. Protects privileged and confidential information. Complies with all Commission policies, administrative and court rules, and state ethics laws. Communicates individually and to small and large groups clearly, concisely, timely, and effectively, both orally and in writing. Works cooperatively\/collaboratively with others.<br><br><em>Applicants<\/em> <em>must<\/em> <em>apply<\/em> <em>through<\/em> <em>the<\/em> <em>City<\/em> <em>of<\/em> <em>Pullman's<\/em> <em>Career<\/em> <em>Portal<\/em> <em>found<\/em> <em>at: <br><br><\/em>https:\/\/www.pullman-wa.gov\/services\/human_resources\/career_portal.php<br><br><strong>The job posting will remain open until filled.<\/strong><br\/><br\/>Please mention the word **ADORER** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Pullman, Pullman, Washington, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-civil-service-secretary-chief-examiner-city-of-pullman-1132560","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-civil-service-secretary-chief-examiner-city-of-pullman-1132560"},{"slug":"remote-research-assistant-neuroscience-research-kennedy-krieger-institute-1132507","id":"1132507","epoch":1780017099,"date":"2026-05-29T01:11:39+00:00","company":"Kennedy Krieger Institute","company_logo":"","position":"Research Assistant Neuroscience Research","tags":["exec","consulting","marketing","travel","c","senior","ops","legal","design","hr","customer support","education","sales","golang","medical","digital nomad","sys admin","video","microsoft","excel","finance","web dev","salesforce","teaching","recruiter","virtual assistant","math","biotech","engineer","part time"],"description":"<strong>Overview<br><br><\/strong>The <strong>Research Assistant I (Part-Time, Remote) <\/strong>in the Opendak Lab will provide dedicated data analysis support for ongoing research projects. This role is fully remote and focused on computational and statistical work, including processing behavioral, electrophysiological, and imaging datasets, contributing to publications and reports, and supporting the analytical needs of the lab.<br><br><strong>Responsibilities<br><br><\/strong><ul><li> Perform statistical analyses on behavioral, electrophysiological, and imaging datasets under direction of the PI.<\/li><li> Process and clean raw data; maintain organized, well-documented data files and analysis pipelines.<\/li><li> Develop figures, graphs, and visualizations of project results for manuscripts, presentations, and grants.<\/li><li> Contribute to preparation of publications, grant reports, and conference presentations based on Opendak Lab research.<\/li><li> Organize, clean, and analyze data in Microsoft Excel; maintain well-structured spreadsheets and analysis files across projects.<\/li><li> Oversee undergraduate data analysts in analysis theory and implementation as needed.<\/li><li> Participate in remote lab meetings and check-ins on a regular schedule to communicate progress and coordinate with team members.<\/li><li> Enhance professional growth and development through educational programs, workshops, and seminars.<br><br><\/li><\/ul><strong>Qualifications<br><br><\/strong>EDUCATION:<br><br>Bachelor's degree in a science-related field (e.g., neuroscience, biology, psychology, computer science, biomedical engineering, mathematics, or statistics) is required.<br><br>EXPERIENCE:<br><br><ul><li> Prior research experience involving data analysis is strongly preferred.<\/li><li> Candidates with demonstrated Excel proficiency and coursework in statistics will be considered.<br><br><\/li><\/ul><strong> Minimum pay range <br><br><\/strong>USD $36,955.98\/Yr.<br><br><strong> Maximum pay range <br><br><\/strong>USD $60,296.50\/Yr.<br\/><br\/>Please mention the word **GRATIFICATION** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Baltimore, ","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-research-assistant-neuroscience-research-kennedy-krieger-institute-1132507","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-research-assistant-neuroscience-research-kennedy-krieger-institute-1132507"},{"slug":"remote-human-resources-coordinator-united-states-slipstream-life-sciences-1132559","id":"1132559","epoch":1780012800,"date":"2026-05-29T00:00:00+00:00","company":"Slipstream Life Sciences","company_logo":"","position":"Human Resources Coordinator United States","tags":["hr","consulting","coordinator","customer support","marketing","payroll","exec","biotech","medical"],"description":"At Slipstream we work to streamline IT Support and provide managed solutions with a strategic consulting and global leadership management approach. Our solutions are designed exclusively for emerging pharma and biotech organizations.<br><br>Slipstream\u00e2\u0080\u0099s industry-leading solutions free clients from the demands of internal IT and allow them to rapidly advance their mission. Led by a leadership team that has been together for over 10 years, you will join a proven team, culture, and strategy to drive innovation within the IT outsourcing industry while developing your skillset with the opportunities for internal growth.<br><br><strong>Job Summary<br><br><\/strong>The Human Resources Coordinator provides administrative support for the Human Resources department. They assist Human Resources Lead with employee records maintenance, onboarding, payroll processing, and providing administrative support to all employees on a daily basis.<br><br><strong>Key Responsibilities<br><br><\/strong><ul><li>Assist with all internal and external Human Resources related inquiries or requests.<\/li><li>Processes new hire onboarding and employee through HRIS.<\/li><li>Hold new hire orientation for all W2 new hires.<\/li><li>Maintain digital copies of employee records in compliance with federal regulations.<\/li><li>Perform I9\/E-Verify &amp; background checks for all W2 new hires.<\/li><li>Assist with performance management procedures.<br><br><\/li><\/ul><strong>Qualifications<br><br><\/strong><ul><li>Bachelor\u00e2\u0080\u0099s degree in human resources or related field, or 3-5 years of experience in lieu of degree.<\/li><li>Full understanding of HR functions and best practices.<\/li><li>Strong analytical skills and highly computer literate with capability in Outlook, MS Office and related business and communications tools.<\/li><li>Meticulous attention to detail a must.<\/li><li>Strong decision-making and problem-solving skills.<\/li><li>Strong organizational and time management skills.<\/li><li>Ability to maintain utmost confidentiality.<br><br><\/li><\/ul><strong>Work Schedule<br><br><\/strong><ul><li>Typical schedule will be Monday to Friday, 8:00 AM to 5:00 PM EST.<\/li><li>Must be flexible to accommodate departmental needs.<br><br><\/li><\/ul><strong>Physical Requirements<br><br><\/strong><ul><li>This position requires the ability to remain in a stationary position, often standing or sitting for prolonged periods.<\/li><li>The ability to move about to accomplish tasks.<\/li><li>Adjusting or moving objects up to 20 pounds in all directions.<\/li><li>Communicating verbally and written word with others to exchange information.<\/li><li>Exposure to a standard office environment with average room temperatures with no adverse environmental conditions expected.<br><br><\/li><\/ul><strong>Benefits<br><br><\/strong><ul><li>401k match<\/li><li>Comprehensive group health, dental, vision benefits<\/li><li>Life insurance\/LTD<\/li><li>Discretionary PTO<\/li><li>Salary: $45,0000-$50,000<br><br><\/li><\/ul><em>Slipstream is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation or identity, national origin, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Slipstream makes hiring decisions based solely on qualifications, merit, and business needs at the time.<br><br><\/em><em>This job description may not be inclusive of all assigned duties, responsibilities, or aspects of the job described, and may be amended at any time at the sole discretion of the Employer.<\/em><br\/><br\/>Please mention the word **RENEWED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Pennsylvania, Pennsylvania, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-human-resources-coordinator-united-states-slipstream-life-sciences-1132559","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-human-resources-coordinator-united-states-slipstream-life-sciences-1132559"},{"slug":"remote-digital-advertising-campaign-manager-tremendous-1132511","id":"1132511","epoch":1779995661,"date":"2026-05-28T19:14:21+00:00","company":"Tremendous","company_logo":"","position":"Digital Advertising Campaign Manager","tags":["exec","consulting","marketing","travel","c","senior","ops","legal","design","hr","customer support","education","sales","golang","medical","digital nomad","sys admin","video","microsoft","excel","finance","web dev","salesforce","teaching","recruiter","virtual assistant","math","biotech","engineer","part time","junior","full time","work from home","testing","dev","quality assurance"],"description":"Tremendous is the global platform built for businesses to send thousands of payouts to anyone, anywhere, for free. We're trusted by 20,000 organizations like Atlassian, MIT, and United Way to deliver gift cards and money to millions of recipients worldwide.<br><br>Our customers (researchers, marketers, HR teams, nonprofits, and platform businesses) rave about how fast and easy Tremendous is to use. Check out our ratings on G2.<br><br>Tremendous is profitable and growing without outside investors. We\u00e2\u0080\u0099re a fully remote, high-documentation, low-meeting culture, which means more time for what matters in both your professional and personal life. The team agrees\u00e2\u0080\u0093 our employee NPS is in the high 80s.<br><br><strong>About The Role<br><br><\/strong>We're looking for a Digital Advertising Campaign Manager to execute and optimize campaigns across paid search, paid social, display, video, and native ad channels within established strategy. This person will partner closely with ad strategists and play a critical role in contributing to pipeline growth.<br><br><strong>You will<br><br><\/strong><ul><li>Own end-to-end campaign execution across paid search, paid social, ABM, and video platforms, including campaign setup, ad refreshes, optimization, QA and ad-hoc reporting<\/li><li>Run and document tests on each platform (such as ad creative, audience, and bidding tests) using a structured test-and-learn approach<\/li><li>Build, launch, and iterate landing page variations using a no-code page builder to achieve conversion, CPA, and ROAS targets<br><br><\/li><\/ul><strong>You have<br><br><\/strong><ul><li>2+ years of hands-on direct platform experience executing paid social, display, video and paid search campaigns<\/li><li>A structured approach to testing; you know how to design a clean experiment and document learnings<\/li><li>Proven success partnering with digital ad strategists to drive value through campaign optimization<\/li><li>Transparent written and verbal communication style<\/li><li>Strong attention to detail and a track record of error-free campaign execution<\/li><li>Comfort using AI tools as a part of process<br><br><\/li><\/ul><strong>Why work with us<br><br><\/strong><ul><li>Competitive pay and equity. Base salary for this role: $80,000 to $110,000.<\/li><li>Real benefits. 100% covered health (US), unlimited PTO, 12-16 weeks paid parental leave.<\/li><li>Fully remote. Work from anywhere in the Americas.<\/li><li>Great culture. Read more about how we work in our public handbook.<\/li><\/ul><br\/><br\/>Please mention the word **SKILLFUL** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"New York, ","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-digital-advertising-campaign-manager-tremendous-1132511","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-digital-advertising-campaign-manager-tremendous-1132511"},{"slug":"remote-news-editor-newsweek-1132508","id":"1132508","epoch":1779987375,"date":"2026-05-28T16:56:15+00:00","company":"Newsweek","company_logo":"","position":"News Editor","tags":["exec","consulting","marketing","travel","c","senior","ops","legal","design","hr","customer support","education","sales","golang","medical","digital nomad","sys admin","video","microsoft","excel","finance","web dev","salesforce","teaching","recruiter","virtual assistant","math","biotech","engineer","part time","junior","full time"],"description":"<p><span>Newsweek is the global media organization that has earned audience time and trust for more than 90 years. Newsweek reaches 100 million people each month with thought-provoking news, opinion, images, graphics, and video delivered across a dozen print and digital platforms. Headquartered in New York City, Newsweek also publishes international editions in EMEA and Asia.\u00c2\u00a0<\/span><\/p><p>\u00c2\u00a0<\/p> <p><strong><span>News Editor, Newsweek.com <\/span><span>\u00c2\u00a0<\/span><\/strong><\/p><p><strong><span>Location: <\/span><\/strong><span>United States (Remote or Hybrid in NYC)<\/span><strong> <\/strong><\/p><p><strong><span>Position Overview:<\/span><\/strong>\u00c2\u00a0<br>The Senior Editor is a senior operational authority in Newsweek\u00e2\u0080\u0099s U.S. newsroom, responsible for setting the editorial bar and enforcing it relentlessly. This role demands editors who can run a national news desk at full throttle\u00e2\u0080\u0094making high-stakes editorial decisions in real time, rewriting aggressively, and delivering journalism that competes head-to-head with the strongest U.S. newsrooms. Reporting to the US News Director, the Senior Editor owns daily execution of the U.S. news report, turning strategy into journalism that is fast, authoritative, analytically sharp, and unmistakably worth a reader\u00e2\u0080\u0099s time. This is a role for editors who expect to touch the most important stories themselves, not manage them from a distance.<\/p><p>This is a full-time position working 3:00 pm-12:00 am ET five days a week, including one weekend shift. This position may be worked remotely anywhere in the United States.<\/p><p><strong><span><span>Key Responsibilities<\/span><span>:<\/span><\/span><\/strong><span>\u00c2\u00a0<\/span><\/p><p><span><strong>Desk Command &amp; Editorial Judgment<\/strong><\/span><\/p><ul><li><span>Run the U.S. news desk during peak coverage hours, making final calls on framing, prioritization, and play. <\/span><\/li><li><span>Distinguish decisively between stories that advance public understanding and those that merely follow the pack. <\/span><\/li><li><span>Kill weak or redundant stories quickly\u00e2\u0080\u0094and demand better replacements. <\/span><\/li><\/ul><p><strong><span>Elite Editing &amp; Rewrite Authority <\/span><\/strong><\/p><ul><li><span>Deliver first-class framing on the most competitive national stories, identifying where Newsweek can add clarity, originality, or analytical value. <\/span><\/li><li><span>Rewrite without hesitation: leads, nut grafs, headlines, structure, sourcing, and tone. <\/span><\/li><li><span>Take raw field notes, transcripts, interviews, and exclusives and turn them into clean, analytical, tightly argued journalism. <\/span><\/li><li><span>Perform rapid second-day and rolling rewrites that materially improve stories as facts evolve. <\/span><\/li><\/ul><p><strong><span>Breaking News &amp; Hands-On Reporting <\/span><\/strong><\/p><ul><li><span>Operate as a desk reporter when the moment demands it\u00e2\u0080\u0094making calls, confirming facts, chasing documents, and closing gaps. <\/span><\/li><li><span>Personally intervene on high-stakes or sensitive stories where precision and judgment are critical. <\/span><\/li><\/ul><p><strong><span>Standards, Culture &amp; Accountability <\/span><\/strong><\/p><ul><li><span>Hold yourself and your team to elite newsroom standards. <\/span><\/li><li><span>Provide blunt, constructive feedback and demand improvement. <\/span><\/li><li><span>Mentor reporters and junior editors into sharper thinkers and stronger journalists. <\/span><\/li><li><span>Take ownership when coverage underperforms. <\/span><\/li><\/ul><p><strong><span>Audience &amp; Competitive Awareness <\/span><\/strong><\/p><ul><li><span>Maintain a sophisticated understanding of how serious readers engage with news. <\/span><\/li><li><span>Work with audience teams to ensure performance goals support editorial ambition. <\/span><\/li><li><span>Monitor competitive coverage and push Newsweek to outperform, not echo.<\/span><\/li><\/ul><p>\u00c2\u00a0<\/p><p><strong><span><span>Qualifications &amp; <\/span><span>Requirements<\/span><span>:\u00c2\u00a0<\/span><\/span><\/strong><span>\u00c2\u00a0<\/span><\/p><ul><li><span>7\u00e2\u0080\u009310+ years of experience at a high-level U.S. digital newsroom. <\/span><\/li><li><span>Demonstrated record editing breaking news, exclusives, and enterprise reporting at speed.<\/span><\/li><li><span>Exceptional news judgment.\u00c2\u00a0<\/span><\/li><li><span>First-rate rewriting skills. <\/span><\/li><li><span>Comfortable making consequential editorial decisions independently. <\/span><\/li><li><span>Proven ability to handle sensitive and legally complex stories. <\/span><\/li><li><span>Deep understanding of U.S. political, legal, and cultural dynamics. <\/span><\/li><li><span>Calm, decisive leadership style under pressure.<\/span><span>\u00c2\u00a0<\/span><\/li><\/ul><p>\u00c2\u00a0<\/p><p><span>Salary Range: $90,000 - $100,000 commensurate with experience.\u00c2\u00a0<\/span><span>\u00c2\u00a0<\/span><\/p> <p><span>Newsweek is an equal opportunity employer. We seek employees of diverse backgrounds and are committed to providing an inclusive, equitable and respectful workplace.<\/span><\/p><br\/><br\/>Please mention the word **INDEBTED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"New York, New York, New York, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-news-editor-newsweek-1132508","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-news-editor-newsweek-1132508"},{"slug":"remote-merchandising-representative-celsius-1132509","id":"1132509","epoch":1779985589,"date":"2026-05-28T16:26:29+00:00","company":"CELSIUS","company_logo":"","position":"Merchandising Representative","tags":["exec","consulting","marketing","travel","c","senior","ops","legal","design","hr","customer support","education","sales","golang","medical","digital nomad","sys admin","video","microsoft","excel","finance","web dev","salesforce","teaching","recruiter","virtual assistant","math","biotech","engineer","part time","junior","full time"],"description":"<p>If\u00c2\u00a0you're\u00c2\u00a0reading this on your way from 5am spin class to festival fast-pass,\u00c2\u00a0you're\u00c2\u00a0CELSIUS\u00c2\u00ae\u00e2\u0080\u0094 an everyday hustler with the essential energy to aim\u00c2\u00a0high, and\u00c2\u00a0go the extra mile wherever your goals take you.\u00c2\u00a0<\/p><p>Joyful by design, sunny by nature, and unapologetically bold. If your bestie has you saved in their phone as \"Icon,\"\u00c2\u00a0you're\u00e2\u0080\u00afALANI NU\u00c2\u00ae\u00e2\u0080\u00af\u00e2\u0080\u0094 confident, colorful, and bringing main-character energy to every moment.\u00c2\u00a0<\/p><p>SoCal in your soul, attitude in your stride. If gravity\u00c2\u00a0doesn't\u00c2\u00a0stop you and \"impossible\" sounds more like \"dare you,\"\u00c2\u00a0you're\u00e2\u0080\u00afROCKSTAR\u00c2\u00ae\u00e2\u0080\u0094 a born rebel, raising the bar with mind-body energy and zero compromise.\u00c2\u00a0<\/p><p>---\u00c2\u00a0<\/p><p>Together,\u00c2\u00a0we're\u00c2\u00a0Celsius Holdings, Inc.\u00e2\u0080\u0094 a global CPG company united by three powerhouse brands and one incredibly talented team.\u00c2\u00a0<\/p><p>At Celsius, we pride ourselves on empowering our people. Every employee has\u00c2\u00a0a stake\u00c2\u00a0in our success. We create a collaborative culture built on inclusivity, innovation, and a belief that great ideas can come from anywhere.\u00c2\u00a0<\/p><p>And\u00c2\u00a0we're\u00c2\u00a0on our way to building something bigger: a category where energy\u00c2\u00a0isn't\u00c2\u00a0just consumed,\u00c2\u00a0it's\u00c2\u00a0lived\u00e2\u0080\u0094where performance meets personality, brand becomes community, and every can crack sparks a statement.\u00c2\u00a0<\/p><p><strong>This is the future of modern energy. This is Celsius.<\/strong>\u00c2\u00a0<\/p><p>\u00c2\u00a0<\/p><p>Ready to take your career to the next level? Join our team and redefine what it means to be energized.\u00c2\u00a0<\/p><p> <em>This is a driving position. A valid U.S. Driver's License required; applicants must pass an MVR (Motor Vehicle Record) screenin<\/em>g. <\/p><p><strong>Pay Rate:\u00c2\u00a0<\/strong>$25\/hour + Overtime (as needed)<\/p><p><strong>Schedule:\u00c2\u00a0Wednesday to Sunday <\/strong><\/p><p><strong>Field-Based:<\/strong>\u00c2\u00a0Role requires presence in assigned market.<\/p><p> <\/p><ul><li><strong>Smyrna, TN<\/strong><\/li><\/ul><strong> <strong>Position Overview<br><br><\/strong><\/strong><p>The Merchandising Representative will report to the Regional Manager and should possess sales qualities, serving as a true ambassador for the Celsius brand across our distribution channels, including grocery, specialty, health club, and convenience stores.<\/p><p>They will be responsible for marketing Celsius products by means of new floor displays\/signage and scheduling demos to attract customers and ensure that shelf space is properly managed.<\/p><p> <\/p><p><strong>Responsibilities <\/strong><\/p><ul><li>Plan and carry out merchandising initiatives<\/li><li>Call on target accounts<\/li><li>Speak with Manager to sell in PDQ's, displays\/end cap placement in store<\/li><li>Communicate sales leads and other incremental opportunities to Celsius territory manager<\/li><li>Expand product distribution as approved by the store manager within the guidelines of the account type<\/li><li>Ensure that account shelves, cold vault and stand-alone coolers are stocked and merchandised according to designated brand flow<\/li><li>Rotate backstock to existing displays, racks, cold space, warm shelf according to account guidelines. (Independent, chain, etc.)<\/li><li>Place point of sales materials as approved by account manager<\/li><li>Participate in new store openings and store reset support<\/li><li>Take pictures; include photos with reporting documents weekly<\/li><li>Conduct demos upon request<\/li><li>Develop and maintain an organized list of target\/key accounts in the territory to help execute weekly \/monthly planning<\/li><li>Communication as needed with territory sales manager\/district manager\/regional manager<\/li><li>Make 15-20 account calls per day<\/li><li>Track and complete all account calls within the Celsius sales app<\/li><li>Submit weekly work logs including mileage<\/li><li>Other records or documentation as assigned<br><br><\/li><\/ul><strong>Requirements<br><br><\/strong><ul><li>Experience: 0-2 years of experience working in retail or merchandising. Prior experience in merchandising a plus<\/li><li>Education: High school diploma or GED<\/li><li>Ability to work flexible hours, 40 hr. work week (Wednesday - Sunday)<\/li><li>Motivated, enthusiastic, and positive attitude<\/li><li>Must be a self-starter and team player<\/li><li>Excellent driving record and insurance\/license required<\/li><li>Personal vehicle to use, an allowance will be provided<\/li><li>Must be committed to providing outstanding customer service<\/li><li>Exceptional interpersonal and communication skills with the ability to interact effectively internally as well as with external contacts<\/li><li>Excellent problem-solving abilities<\/li><li>Ability to multi-task within a fast-paced industry<\/li><li>Candidate must live in within their county area<br><br><\/li><\/ul><strong>Benefits<br><br><\/strong><ul><li>Comprehensive Medical, Dental &amp; Vision benefits<\/li><li>Long- and short-term disability<\/li><li>Life insurance<\/li><li>10 Vacation days per year subject to accrual policy<\/li><li>11 Company paid holidays<\/li><li>401(k) with Company match<\/li><li>Identity theft and legal services<br><\/li><\/ul><p><em>Celsius Holdings, Inc. celebrates diversity and is committed to creating an inclusive environment for all employees. We are proud to provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. We believe strongly in fostering a safe, fair and respectful work environment. If you need assistance and\/or a reasonable accommodation due to a disability during the application process, please reach out to careers@celsius.com.<br><br>The above information has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job.<\/em><\/p><br\/><br\/>Please mention the word **SIMPLIFYING** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Smyrna, Smyrna, Tennessee, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-merchandising-representative-celsius-1132509","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-merchandising-representative-celsius-1132509"},{"slug":"remote-guest-experience-specialist-work-from-home-co-1132510","id":"1132510","epoch":1779909998,"date":"2026-05-27T19:26:38+00:00","company":"Work From Home Co.","company_logo":"","position":"Guest Experience Specialist","tags":["exec","consulting","marketing","travel","c","senior","ops","legal","design","hr","customer support","education","sales","golang","medical","digital nomad","sys admin","video","microsoft","excel","finance","web dev","salesforce","teaching","recruiter","virtual assistant","math","biotech","engineer","part time","junior","full time","work from home"],"description":"This is a remote position.<br><br>We are seeking a motivated and detail-oriented <strong>Remote Guest Experience Specialist<\/strong> to join our remote team. In this role, you will assist customers with inquiries, scheduling, account updates, and service coordination while delivering a high level of professionalism and care. This position is ideal for someone who enjoys helping people, solving problems, and working in a fast-paced remote environment. You will serve as a key point of contact for customers, ensuring a smooth and positive experience from initial request through follow-up support.<br><br><strong>Requirements<br><br><\/strong><ul><li>Previous experience in customer service, hospitality, call center, or administrative roles preferred <\/li><li>Strong written and verbal communication skills <\/li><li>Comfortable working independently in a remote environment <\/li><li>Basic computer skills and ability to learn new systems quickly <\/li><li>Reliable internet connection and a distraction-free workspace <\/li><li>Strong attention to detail and organizational skills <\/li><li>Positive attitude and solution-focused mindset <br><br><\/li><\/ul>Key Responsibilities<br><br><ul><li>Respond to customer inquiries via email, chat, and phone in a timely and professional manner <\/li><li>Assist with service requests, scheduling updates, and general account support <\/li><li>Provide clear information about available services and options <\/li><li>Maintain accurate records using internal systems and CRM tools <\/li><li>Resolve basic customer concerns and escalate complex issues when necessary <\/li><li>Follow internal processes to ensure quality and consistency <\/li><li>Support team initiatives and ongoing customer experience improvements <br><br><\/li><\/ul><strong>Benefits<br><br><\/strong>Benefits<br><br><ul><li>Remote work flexibility <\/li><li>Competitive pay with performance-based opportunities <\/li><li>Flexible scheduling options <\/li><li>Ongoing training and professional development <\/li><li>Supportive and collaborative team environment <\/li><li>Advancement opportunities based on performance <br><br><\/li><\/ul><strong>Equal Opportunity <br><br><\/strong>We celebrate diversity and are committed to creating an inclusive environment for all team members. All qualified applicants will be considered without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, or disability.<br><br><br\/><br\/>Please mention the word **ENHANCED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"New York, New York, New York, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-guest-experience-specialist-work-from-home-co-1132510","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-guest-experience-specialist-work-from-home-co-1132510"},{"slug":"remote-associate-chief-of-staff-the-co-founders-radicle-science-1132352","id":"1132352","epoch":1779844693,"date":"2026-05-27T01:18:13+00:00","company":"Radicle Science","company_logo":"","position":"Associate Chief of Staff the Co Founders","tags":["embedded","sys admin","infosec","education","technical","coordinator","customer support","dev","testing","marketing","travel","speech","exec","payroll","video","cloud","microsoft","ops","excel","stats","medical","recruiter","full time","digital nomad","project manager","finance","junior","virtual assistant","senior","biotech"],"description":"<p>Radicle Science is seeking an exceptional, AI-native Associate Chief of Staff to serve as a force multiplier to Co-Founders Pelin Thorogood and Dr. Jeff Chen.<\/p><p>This is a high-leverage, founder-facing role designed for a high-ceiling operator ready to grow into strategic leadership as Radicle scales. You may come from an executive assistant, executive operations, founder associate, project management, or operations background. This is not a traditional administrative role \u00e2\u0080\u0094 it blends executive operations, founder leverage, project coordination, AI-enabled systems building, and strategic follow-through.<\/p><p>The right person thrives in dynamic environments, brings order to complexity, and moves with urgency, judgment, and creativity. After meetings, you've already reviewed the notes, identified priorities, drafted follow-ups, updated trackers, and moved the work forward \u00e2\u0080\u0094 without being asked.<\/p><p><strong>This role is built for the AI era.<\/strong> You will use agentic AI \u00e2\u0080\u0094 Claude, ChatGPT, workflow automation, and emerging tools \u00e2\u0080\u0094 not as a nice-to-have, but as your core operating system. You'll be expected to 10x your own output through AI and help build the operational infrastructure that lets Radicle move faster than companies 10x our size. If you're not already experimenting with AI agents, automations, and LLM-powered workflows in your daily work, this role is probably not for you.<\/p><strong>WHAT YOU\u00e2\u0080\u0099LL DO: ESSENTIAL DUTIES AND RESPONSIBILITIES<\/strong><strong>Founder Leverage &amp; Executive Operations<\/strong><ul><li><span>Own and continuously optimize the operating rhythm of the co-founders, including calendars, inboxes, meeting preparation, travel, communications, and priority management<\/span><\/li><li><span>Ensure Pelin and Jeff are fully prepared for high-stakes meetings with agendas, materials, context, desired outcomes, and follow-up plans<\/span><\/li><li><span>Dynamically prioritize and re-prioritize based on evolving business needs, strategic importance, and founder bandwidth<\/span><\/li><li><span>Draft polished communications, manage timely follow-through, and help ensure critical relationships and priorities do not fall through the cracks<\/span><\/li><\/ul><strong>AI-Enabled Productivity &amp; Systems<\/strong><ul><li><span>Use AI tools, LLMs, agentic workflows, and automations to plan, draft, synthesize, organize, and accelerate execution<\/span><\/li><li><span>Build and continuously improve AI-enabled systems that multiply executive and organizational productivity<\/span><\/li><li><span>Identify and implement opportunities to automate repetitive workflows across scheduling, communications, meeting notes, research, reporting, and follow-up<\/span><\/li><li><span>Continuously explore, evaluate, and deploy new AI tools and workflows that help Radicle move at the speed of AI<\/span><\/li><li><span>Help establish Radicle\u00e2\u0080\u0099s internal playbook for AI-augmented operations<\/span><\/li><\/ul><strong>Operating Rhythm &amp; Strategic Follow-Through<\/strong><ul><li><span>Track key meetings, decisions, action items, owners, deadlines, and next steps to ensure momentum and accountability<\/span><\/li><li><span>Independently review meeting notes \u00e2\u0080\u0094 including AI-generated summaries \u00e2\u0080\u0094 identify priorities, and drive follow-up without needing detailed direction<\/span><\/li><li><span>Support the cadence of leadership meetings, company rocks, strategic initiatives, board preparation, investor follow-ups, hiring priorities, partnerships, and other founder-led projects<\/span><\/li><li><span>Translate conversations into decisions, owners, next steps, and accountability loops<\/span><\/li><\/ul><strong>Project &amp; Cross-Functional Coordination<\/strong><ul><li><span>Support cross-functional projects led by Pelin and Jeff from planning through execution<\/span><\/li><li><span>Coordinate across internal stakeholders to reduce friction, surface blockers, and keep priorities moving<\/span><\/li><li><span>Prepare high-quality materials for leadership meetings, retreats, board interactions, investor discussions, and strategic initiatives<\/span><\/li><li><span>Serve as a central coordination point for direct reports, leadership team members, advisors, partners, and other key stakeholders<\/span><\/li><\/ul><strong>Travel, Events &amp; Relationship Management<\/strong><ul><li><span>Coordinate seamless business and occasional personal travel, including flights, accommodations, itineraries, and related logistics<\/span><\/li><li><span>Plan and execute high-quality internal and external events, including venue selection, guest experience, logistics, and menu planning<\/span><\/li><li><span>Maintain and organize key relationships across investors, partners, advisors, clients, prospects, and external stakeholders<\/span><\/li><li><span>Represent Radicle with polish, warmth, discretion, and strong judgment<\/span><\/li><\/ul><p><br><\/p><strong>WHAT YOU\u00e2\u0080\u0099LL BRING: REQUIRED QUALIFICATIONS<\/strong><ul><li><span>4\u00e2\u0080\u00938+ years of experience in executive support, executive operations, founder support, project management, operations, or a similar high-leverage role<\/span><\/li><li><span>Experience supporting senior executives, founders, or fast-moving leaders in high-growth environments<\/span><\/li><li><span>Demonstrated ability to use AI agents and LLMs to independently plan, execute, and iterate on complex workflows \u00e2\u0080\u0094 not just prompting, but building systems and agentic workflows that multiply your output<\/span><\/li><li><span>Exceptional organization, prioritization, time management, and follow-through<\/span><\/li><li><span>Strong written and verbal communication skills, with the ability to draft polished, thoughtful, and context-aware communications<\/span><\/li><li><span>High discretion, professionalism, judgment, and emotional intelligence<\/span><\/li><li><span>A strong bias toward action, ownership, and closing loops<\/span><\/li><li><span>Curiosity, adaptability, and eagerness to continuously learn, experiment, and optimize<\/span><\/li><li><span>Comfort operating in ambiguity, change, and speed<\/span><\/li><\/ul><p><br><\/p><strong>PREFERRED SKILLS AND EXPERIENCE<\/strong><ul><li><span>Experience in startups, healthtech, biotech, wellness, technology, or other high-growth environments<\/span><\/li><li><span>Exposure to Chief of Staff-like responsibilities, executive operations, project management, or internal operating systems<\/span><\/li><li><span>Familiarity with EOS or similar organizational models<\/span><\/li><li><span>Experience supporting multiple executives simultaneously<\/span><\/li><li><span>Comfort with tools such as Google Workspace, Slack, Notion, ChatGPT, Claude, CoWork, project management platforms, and other AI-enabled productivity tools<\/span><\/li><li><span>Experience building automated workflows or integrating AI tools into operational processes<br><\/span><\/li><\/ul><strong>COMPENSATION &amp; GROWTH<\/strong><p><span>This is a ground-floor opportunity to grow with a company recognized by Inc. 5000 as one of America\u00e2\u0080\u0099s fastest-growing companies and by Fast Company as a \u00e2\u0080\u009cWorld Changing Idea\u00e2\u0080\u009d and \u00e2\u0080\u009cMost Innovative Workplace.\u00e2\u0080\u009d<\/span><\/p><ul><li><span>Base Salary: $80,000\u00e2\u0080\u0093$100,000 (depending on experience)<\/span><\/li><li><span>Performance-Based Bonus<\/span><\/li><li><span>Equity: Meaningful equity stake in a high-growth healthtech company<\/span><\/li><li><span>Clear path from operational leadership to strategic leadership as Radicle scales<\/span><\/li><\/ul><p><span>We\u00e2\u0080\u0099re looking for someone who sees this role not as a job, but as a launchpad \u00e2\u0080\u0094 someone who wants to grow alongside a company building something that will permanently alter the course of health and wellness for all future generations.<\/span><\/p><p><br><\/p><strong>WORKING STYLE<\/strong><p><span>You are highly proactive, exceptionally organized, detail-oriented, dependable, polished, calm under pressure, creatively resourceful, and energized by getting things done.<\/span><\/p><p><span>You love being at the center of the action, connecting dots, anticipating needs, creating clarity, and helping high-impact leaders move faster and better.<\/span><\/p><p><span>This is not a traditional corporate Chief of Staff role where the work is primarily strategy decks and executive advising from a distance. It is a hands-on, high-ownership role where you may move from drafting a board follow-up, to preparing a founder for an investor meeting, to cleaning up a messy workflow, to coordinating a leadership offsite \u00e2\u0080\u0094 sometimes in the same day.<\/span><\/p><p><span>This is a remote-first role with flexibility, with a strong preference for candidates based on the West Coast, ideally in Southern California. The person in this role must be able to work West Coast hours and travel to San Diego approximately 4\u00e2\u0080\u00936 times per year for company meetings, leadership sessions, and other key in-person gatherings.<\/span><\/p><p><span>If you are looking for a predictable 8\u00e2\u0080\u00935 role with static responsibilities, this is probably not the right fit. If you are excited by speed, mission, trust, variety, AI-enabled leverage, and the opportunity to grow with a category-defining company, this could be an extraordinary role.<\/span><\/p><p><br><\/p>About Radicle Science<p>Radicle Science is a healthtech pioneer named Fast Company \"World Changing Idea\" for creating the future of proven, precision wellness. Since 2021, Radicle has become the #1 global leader in rigorous clinical evidence generation for wellness \u00e2\u0080\u0094 running placebo-controlled trials on more Americans annually than all FDA drug-approval trials combined. We fuse AI, consumer science, and decentralized trials to generate unprecedented data at speed and scale. Our fully automated, vertically integrated platform enables clients to build portfolios of patentable, proven, precision wellness formulas \u00e2\u0080\u0094 trusted by consumers, retailers, regulators, healthcare providers, and AI models.<\/p><p><strong>Our 10-year vision:<\/strong> A world where 1 billion people dramatically improve their health every day with precision wellness solutions proven by Radicle Science.<\/p>Culture<p>We seek <strong>Rebels With a Cause<\/strong> \u00e2\u0080\u0094 team members who are both a skill fit and a values fit. Our core values:<\/p><ul><li><strong>Rebel with a Cause<\/strong> \u00e2\u0080\u0094 Challenge the status quo, anchored in mission and integrity<\/li><li><strong>Audacious (without the ego)<\/strong> \u00e2\u0080\u0094 Swing big, iterate fast, don't wait for perfect<\/li><li><strong>GSD<\/strong> \u00e2\u0080\u0094 Take ownership, follow through, deliver reliably<\/li><li><strong>Evidence-Driven<\/strong> \u00e2\u0080\u0094 Test, measure, learn, improve<\/li><li><strong>Grounded Brilliance<\/strong> \u00e2\u0080\u0094 Sharp and humble; curious, respectful, collaborative<\/li><li><strong>Transparent<\/strong> \u00e2\u0080\u0094 Communicate clearly and candidly so trust stays high<\/li><\/ul>The Team<p>Radicle is a team of 35+ Rebels, co-founded in 2020 by <strong>Pelin Thorogood<\/strong>, M.Eng\/MBA (tech founder, INC 200 Female Founder, Trustee &amp; Vice Chair of UCSD Foundation) and <strong>Dr. Jeff Chen<\/strong>, MD\/MBA (physician-scientist, founded and led UCLA's natural products research center). Advisors include Peter Diamandis (Fortune \"50 Greatest World Leaders\"), Dr. Jonathan Fielding (UCLA Fielding School of Public Health, White House Advisor), and Pamela Harbour (former FTC Commissioner).<\/p><p><em>The work will be hard \u00e2\u0080\u0094 but if we succeed, we will permanently alter the course of health and wellness for all future generations.<\/em><\/p><br\/><br\/>Please mention the word **IMPECCABLE** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"California, California, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-chief-of-staff-the-co-founders-radicle-science-1132352","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-chief-of-staff-the-co-founders-radicle-science-1132352"},{"slug":"remote-community-associate-draftkings-inc-1132355","id":"1132355","epoch":1779833153,"date":"2026-05-26T22:05:53+00:00","company":"DraftKings Inc.","company_logo":"","position":"Community Associate","tags":["embedded","sys admin","infosec","education","technical","coordinator","customer support","dev","testing","marketing","travel","speech","exec","payroll","video","cloud","microsoft","ops","excel","stats","medical","recruiter","full time","digital nomad","project manager","finance","junior","virtual assistant","senior","biotech","teaching","game dev","content writing"],"description":"At DraftKings, AI is becoming an integral part of both our present and future, powering how work gets done today, guiding smarter decisions, and sparking bold ideas. It\u00e2\u0080\u0099s transforming how we enhance customer experiences, streamline operations, and unlock new possibilities. Our teams are energized by innovation and readily embrace emerging technology. We\u00e2\u0080\u0099re not waiting for the future to arrive. We\u00e2\u0080\u0099re shaping it, one bold step at a time. To those who see AI as a driver of progress, come build the future together.<br><br>The Crown Is Yours<br><br>We are looking for a Community Associate to help us build the most engaged, trusted, and exciting sportsbook community in the game. You\u00e2\u0080\u0099ll be on the front lines of our official Discord server, helping connect, support, and energize our players every day. In this hands-on, execution-focused role, you'll work closely with the Community Lead to bring our brand to life through conversations, content, and events that matter to our players.<br><br>What you'll do<br><br><ul><li>Be an everyday presence in our Discord server, engaging authentically with our players across channels, topics, and live sports moments.<\/li><li>Serve as a trusted point of contact, responding quickly and helpfully to player questions and needs.<\/li><li>Create and execute community-first campaigns including giveaways, AMAs, live chats, and themed events in partnership with internal and external teams.<\/li><li>Monitor sentiment, player behavior, and emerging trends, and share insights regularly to improve products, features, and the overall experience.<\/li><li>Champion the community\u00e2\u0080\u0099s voice across the company while upholding our brand tone and standards.<\/li><li>Support coverage during sports-heavy periods \u00e2\u0080\u0094 evenings, weekends, and big game days (on rotation).<br><br><br><\/li><\/ul>What you'll bring<br><br><ul><li>At least 1 year of experience building, moderating, or supporting digital communities; preferably around sports, gaming, or consumer brands.<\/li><li>Deep familiarity with Discord, including mod tools, roles, bots, and engagement features.<\/li><li>Proven ability to create thumb-stopping content and conversations tailored to specific communities.<\/li><li>Excellent written communication skills with a flexible tone: professional, playful, empathetic \u00e2\u0080\u0094 whatever the moment calls for.<\/li><li>A strong sense of urgency and ownership \u00e2\u0080\u0094 you\u00e2\u0080\u0099re fast, proactive, and solutions-focused.<\/li><li>An understanding of Sportsbook or Daily Fantasy Sports products and can talk betting lines, big games, or prop picks without missing a beat.<\/li><li>Experience moderating high-volume communities or social platforms during live events is a plus.<\/li><li>Knowledge of responsible gaming practices and customer safety.<br><br><br><\/li><\/ul>#AC2025<br><br>Join Our Team<br><br>We\u00e2\u0080\u0099re a publicly traded (NASDAQ: DKNG) technology company headquartered in Boston. As a regulated gaming company, you may be required to obtain a gaming license issued by the appropriate state agency as a condition of employment. Don\u00e2\u0080\u0099t worry, we\u00e2\u0080\u0099ll guide you through the process if this is relevant to your role.<br><br>The US base salary range for this full-time position is 56,300.00 USD - 70,400.00 USD, plus bonus, equity, and benefits as applicable. Our ranges are determined by role, level, and location. The compensation information displayed on each job posting reflects the range for new hire pay rates for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific pay range and how that was determined during the hiring process. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.<br><br><br\/><br\/>Please mention the word **REGALLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Massachusetts, Massachusetts, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-community-associate-draftkings-inc-1132355","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-community-associate-draftkings-inc-1132355"},{"slug":"remote-customer-service-representative-cigna-healthcare-cigna-healthcare-1132353","id":"1132353","epoch":1779753600,"date":"2026-05-26T00:00:00+00:00","company":"Cigna Healthcare","company_logo":"","position":"Customer Service Representative Cigna Healthcare","tags":["embedded","sys admin","infosec","education","technical","coordinator","customer support","dev","testing","marketing","travel","speech","exec","payroll","video","cloud","microsoft","ops","excel","stats","medical","recruiter","full time","digital nomad","project manager","finance","junior","virtual assistant","senior","biotech"],"description":"<strong>Summary\u00e2\u0080\u00af<br><br><\/strong>The Cigna Group is a global Health Service company that is dedicated to helping people improve their health and vitality. Our <strong>Medical Proclaim Provider<\/strong> team seeks dedicated, compassionate, and empathetic <strong>Customer Service Representatives,<\/strong> who are genuinely interested in helping people at some critical points of their lives, to join our team. The Call Center Customer Service Representative represents the company, and our people make all the difference in our success.\u00e2\u0080\u00af<br><br>\u00e2\u0080\u00af<br><br><strong>Responsibilities<br><br><\/strong><ul><li>Answer inbound calls from health care providers with inquiries regarding medical claims, benefits, appeals, prior authorizations, and medical codes.<\/li><li>An average of 50+ calls are expected daily.\u00e2\u0080\u00af\u00e2\u0080\u00af <\/li><li>Take inbound calls while toggling through several applications on multiple screens.\u00e2\u0080\u00af\u00e2\u0080\u00af <\/li><li>Attend 100% of trainings, and the first 90 days of employment.\u00e2\u0080\u00af\u00e2\u0080\u00af <\/li><li>Resolve customer complaints through independent problem-solving skills and one-call resolution.\u00e2\u0080\u00af\u00e2\u0080\u00af <\/li><li>Understand and strive to meet or exceed call center metrics while providing excellent consistent customer service.\u00e2\u0080\u00af\u00e2\u0080\u00af <br><br><\/li><\/ul>\u00e2\u0080\u00af<br><br><strong>Qualifications\u00e2\u0080\u00af<br><br><\/strong><ul><li>High School diploma or equivalent\u00e2\u0080\u00af <\/li><li>1 year of customer service experience is required\u00e2\u0080\u00af <\/li><li>A dedicated workspace with no distractions is required\u00e2\u0080\u00af <\/li><li>Intermediate proficiency in Microsoft Outlook<\/li><li>Knowledge of Medical Terminology a PLUS<\/li><li>Excellent written and oral communication skills<br><br><\/li><\/ul>If you will be working at home occasionally or permanently, the internet connection must be obtained through a cable broadband or fiber optic internet service provider with speeds of at least 10Mbps download\/5Mbps upload.<br><br><strong>About The Cigna Group<br><br><\/strong>Doing something meaningful starts with a simple decision, a commitment to changing lives. At The Cigna Group, we\u00e2\u0080\u0099re dedicated to improving the health and vitality of those we serve. Through our divisions Cigna Healthcare and Evernorth Health Services, we are committed to enhancing the lives of our clients, customers and patients. Join us in driving growth and improving lives.<br><br><em>Qualified applicants will be considered without regard to race, color, age, disability, sex, childbirth (including pregnancy) or related medical conditions including but not limited to lactation, sexual orientation, gender identity or expression, veteran or military status, religion, national origin, ancestry, marital or familial status, genetic information, status with regard to public assistance, citizenship status or any other characteristic protected by applicable equal employment opportunity laws.<br><br><\/em><em>If you need a reasonable accommodation to complete the online application process, please email <\/em><em><strong>seeyourself@thecignagroup.com<\/strong><\/em><em> for assistance. Please note that this email inbox is dedicated to accommodation requests only and cannot provide application updates or accept resumes.<br><br><\/em><em>The Cigna Group has a tobacco-free policy and reserves the right not to hire tobacco\/nicotine users in states where that is legally permissible. Candidates in such states who use tobacco\/nicotine will not be considered for employment unless they enter a qualifying smoking cessation program prior to the start of their employment. These states include: Alabama, Alaska, Arizona, Arkansas, Delaware, Florida, Georgia, Hawaii, Idaho, Iowa, Kansas, Maryland, Massachusetts, Michigan, Nebraska, Ohio, Pennsylvania, Texas, Utah, Vermont, and Washington State.<br><br><\/em><em>Qualified applicants with criminal histories will be considered for employment in a manner consistent with all federal, state and local ordinances.<\/em><br\/><br\/>Please mention the word **PAINLESS** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Tennessee, Tennessee, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-customer-service-representative-cigna-healthcare-cigna-healthcare-1132353","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-customer-service-representative-cigna-healthcare-cigna-healthcare-1132353"},{"slug":"remote-educator-tutor-me-la-llc-1132354","id":"1132354","epoch":1779705619,"date":"2026-05-25T10:40:19+00:00","company":"Tutor Me LA LLC","company_logo":"","position":"Educator","tags":["embedded","sys admin","infosec","education","technical","coordinator","customer support","dev","testing","marketing","travel","speech","exec","payroll","video","cloud","microsoft","ops","excel","stats","medical","recruiter","full time","digital nomad","project manager","finance","junior","virtual assistant","senior","biotech","teaching"],"description":"Tutor Me Education is reshaping how students learn. We are looking for teachers and tutors with virtual tutoring experience to provide 1:1 or group instruction to students all across the country!<br><br>Here are the details:<br><br><ul><li>Virtual instruction from your home computer, on your schedule! This is a remote job!<\/li><li>Set your own availability and change it at any time<\/li><li>Set your own hourly rate and negotiate on a per job basis<\/li><li>We will ask you to share the subjects you can teach the best, and systematically send jobs to your email based on those subjects<br><br><\/li><\/ul>About Tutor Me Education:<br><br><ul><li>We are a tutoring and test-preparation platform that connects tutors with clients and school districts<\/li><li>Tutors set their own hourly rate and decide which tutoring jobs to accept based on their availability<\/li><li>At Tutor Me Education, there are always new job opportunities with hundreds of new students signing up every day!<br><br><\/li><\/ul><strong>Requirements<br><br><\/strong>Job requirements:<br><br><ul><li>Previous tutoring\/teaching experience highly preferred<\/li><li>Previous experience with special education, accommodations, and working with students with learning disabilities highly preferred<\/li><li>At least a Bachelor's degree<\/li><li>Ability to make learning fun and interactive, with the focus of the tutoring often determined by student questions and comments<\/li><li>Ability to pass a background check if required<\/li><li>This is a contract job, with opportunities for additional tutoring\/virtual instruction thereafter. Tutors and teachers on our platform systematically receive opportunities as they come in based on experience, subjects offered, availability, etc<br><br><\/li><\/ul><strong>Benefits<br><br><\/strong>Flexible schedule!<br><br>Work from home on your personal computer!<br><br>Set your own hourly rate!<br\/><br\/>Please mention the word **IMPRESSIVENESS** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Los Angeles, Los Angeles, California, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-educator-tutor-me-la-llc-1132354","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-educator-tutor-me-la-llc-1132354"},{"slug":"remote-junior-front-end-developer-pulsemedia-apac-1132223","id":"1132223","epoch":1779494400,"date":"2026-05-23T00:00:00+00:00","company":"PULSEMEDIA (APAC)","company_logo":"","position":"Junior Front End Developer","tags":["analyst","technical","customer support","marketing","accounting","finance","education","exec","excel","legal","virtual assistant","video","microsoft","ops","saas","cloud","sales","recruiter","data entry","admin","front end","dev","design","react","wordpress","full stack","testing","web dev","javascript","css","git","seo","mobile","content writing","senior","junior","sys admin","medical","engineer","digital nomad","writer","travel","speech","ecommerce","biotech"],"description":"This role is perfect for a motivated and creative developer who is passionate about building exceptional digital experiences and eager to grow in a fast-paced, healthcare-focused environment. You\u00e2\u0080\u0099ll collaborate closely with designers, marketers, and developers to create high-quality web solutions for healthcare and medical clients.<br><br>If you enjoy front-end development, modern web technologies, and turning ideas into engaging user experiences, we\u00e2\u0080\u0099d love to hear from you.<br><br>Key Responsibilities<br><br>Front-End Development<br><br><ul><li>Build and maintain responsive, user-friendly websites and interfaces for healthcare and medical clients.<\/li><li>Convert UI\/UX designs into clean, scalable, and reusable front-end code.<\/li><li>Support the development of landing pages, websites, and digital marketing assets.<br><br><\/li><\/ul>Collaboration &amp; Teamwork<br><br><ul><li>Work closely with designers, marketers, and project managers to deliver seamless user experiences.<\/li><li>Assist with implementing front-end improvements related to SEO, CRO, and website performance.<br><br><\/li><\/ul>Website Optimization<br><br><ul><li>Optimize websites for speed, responsiveness, and cross-browser compatibility.<\/li><li>Ensure websites function smoothly across desktop, tablet, and mobile devices.<\/li><li>Follow accessibility and usability best practices.<br><br><\/li><\/ul>CMS &amp; Website Maintenance<br><br><ul><li>Maintain and update websites built on CMS platforms such as WordPress.<\/li><li>Implement content updates, layouts, and page templates based on client and internal requirements.<br><br><\/li><\/ul>Quality Assurance &amp; Debugging<br><br><ul><li>Identify and resolve front-end bugs and UI inconsistencies.<\/li><li>Test websites and features across multiple browsers and devices to ensure reliability.<br><br><\/li><\/ul>Learning &amp; Growth<br><br><ul><li>Stay current with modern front-end technologies, frameworks, and industry best practices.<\/li><li>Participate in code reviews and actively learn from senior developers and team feedback.<br><br><\/li><\/ul><strong>Experience<br><br><\/strong>Required Qualifications<br><br><ul><li>0\u00e2\u0080\u00932 years of front-end development experience (internships, freelance work, and personal projects are welcome).<\/li><li>Experience building real-world websites or web applications is a plus.<br><br><\/li><\/ul>Education<br><br><ul><li>Bachelor\u00e2\u0080\u0099s degree in Computer Science, Software Engineering, Web Development, or a related field \u00e2\u0080\u0094 or equivalent practical experience.<br><br><\/li><\/ul>Technical Skills<br><br><ul><li>Strong understanding of HTML5, CSS3, and JavaScript.<\/li><li>Familiarity with responsive and mobile-first development principles.<\/li><li>Basic knowledge of front-end frameworks or libraries such as React or Vue is a plus.<\/li><li>Experience with WordPress or similar CMS platforms is preferred.<\/li><li>Understanding of SEO-friendly front-end practices.<br><br><\/li><\/ul>Tools &amp; Technologies<br><br><ul><li>Familiarity with version control systems such as Git.<\/li><li>Experience working with design collaboration tools like Figma or Adobe XD.<\/li><li>Basic understanding of performance optimization and browser compatibility.<br><br><\/li><\/ul>Soft Skills<br><br><ul><li>Strong attention to detail and problem-solving abilities.<\/li><li>Good communication skills and ability to collaborate in a remote team environment.<\/li><li>Positive attitude toward learning, feedback, and professional growth.<\/li><li>Strong time management and organizational skills.<br><br><\/li><\/ul><strong>Preferred Qualifications<br><br><\/strong><ul><li>Experience with Tailwind CSS, Bootstrap, or similar CSS frameworks.<\/li><li>Basic understanding of accessibility standards (WCAG).<\/li><li>Exposure to healthcare, medical, or regulated industries is a plus.<\/li><li>Familiarity with JavaScript tooling and front-end workflows.<\/li><li>Fluent English communication skills; Arabic is a strong advantage.<br><br><\/li><\/ul>Why Join PulseMediaNL?<br><br>Competitive Compensation<br><br><ul><li>Competitive salary based on experience and skills.<\/li><li>Paid holidays and time off based on your country of residence.<br><br><\/li><\/ul>Professional Growth<br><br><ul><li>Mentorship from experienced developers and designers.<\/li><li>Opportunities to grow into mid-level front-end or full-stack development roles.<\/li><li>Hands-on experience with international healthcare and digital marketing projects.<br><br><\/li><\/ul>Fully Remote Environment<br><br><ul><li>Work remotely from anywhere in the MENA region.<\/li><li>Flexible working hours that support work-life balance.<\/li><li>Collaborative remote-first culture with modern tools and workflows.<br><br><\/li><\/ul>Supportive &amp; Innovative Culture<br><br><ul><li>Join a creative and forward-thinking team that values innovation, quality, and collaboration.<\/li><li>Work in an environment that encourages continuous learning and professional development.<br><br><\/li><\/ul>Meaningful Work<br><br><ul><li>Help build digital solutions that positively impact healthcare and wellness industries across local and global markets.<br><br><\/li><\/ul>How to Apply<br><br>If you\u00e2\u0080\u0099re a motivated Junior Front-End Developer based in the MENA region and excited to grow your career within a healthcare-focused digital agency, we\u00e2\u0080\u0099d love to hear from you.<br><br>Please submit your resume and portfolio (if available).<br><br>We are an equal opportunity employer. We welcome applicants from all backgrounds and value diverse perspectives and experiences.<br\/><br\/>Please mention the word **INTELLIGENT** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Makkah Region","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-junior-front-end-developer-pulsemedia-apac-1132223","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-junior-front-end-developer-pulsemedia-apac-1132223"},{"slug":"remote-junior-front-end-developer-pulsemedia-apac-1132224","id":"1132224","epoch":1779494400,"date":"2026-05-23T00:00:00+00:00","company":"PULSEMEDIA (APAC)","company_logo":"","position":"Junior Front End Developer","tags":["analyst","technical","customer support","marketing","accounting","finance","education","exec","excel","legal","virtual assistant","video","microsoft","ops","saas","cloud","sales","recruiter","data entry","admin","front end","dev","design","react","wordpress","full stack","testing","web dev","javascript","css","git","seo","mobile","content writing","senior","junior","sys admin","medical","engineer","digital nomad","writer","travel","speech","ecommerce","biotech"],"description":"This role is perfect for a motivated and creative developer who is passionate about building exceptional digital experiences and eager to grow in a fast-paced, healthcare-focused environment. You\u00e2\u0080\u0099ll collaborate closely with designers, marketers, and developers to create high-quality web solutions for healthcare and medical clients.<br><br>If you enjoy front-end development, modern web technologies, and turning ideas into engaging user experiences, we\u00e2\u0080\u0099d love to hear from you.<br><br>Key Responsibilities<br><br>Front-End Development<br><br><ul><li>Build and maintain responsive, user-friendly websites and interfaces for healthcare and medical clients.<\/li><li>Convert UI\/UX designs into clean, scalable, and reusable front-end code.<\/li><li>Support the development of landing pages, websites, and digital marketing assets.<br><br><\/li><\/ul>Collaboration &amp; Teamwork<br><br><ul><li>Work closely with designers, marketers, and project managers to deliver seamless user experiences.<\/li><li>Assist with implementing front-end improvements related to SEO, CRO, and website performance.<br><br><\/li><\/ul>Website Optimization<br><br><ul><li>Optimize websites for speed, responsiveness, and cross-browser compatibility.<\/li><li>Ensure websites function smoothly across desktop, tablet, and mobile devices.<\/li><li>Follow accessibility and usability best practices.<br><br><\/li><\/ul>CMS &amp; Website Maintenance<br><br><ul><li>Maintain and update websites built on CMS platforms such as WordPress.<\/li><li>Implement content updates, layouts, and page templates based on client and internal requirements.<br><br><\/li><\/ul>Quality Assurance &amp; Debugging<br><br><ul><li>Identify and resolve front-end bugs and UI inconsistencies.<\/li><li>Test websites and features across multiple browsers and devices to ensure reliability.<br><br><\/li><\/ul>Learning &amp; Growth<br><br><ul><li>Stay current with modern front-end technologies, frameworks, and industry best practices.<\/li><li>Participate in code reviews and actively learn from senior developers and team feedback.<br><br><\/li><\/ul><strong>Experience<br><br><\/strong>Required Qualifications<br><br><ul><li>0\u00e2\u0080\u00932 years of front-end development experience (internships, freelance work, and personal projects are welcome).<\/li><li>Experience building real-world websites or web applications is a plus.<br><br><\/li><\/ul>Education<br><br><ul><li>Bachelor\u00e2\u0080\u0099s degree in Computer Science, Software Engineering, Web Development, or a related field \u00e2\u0080\u0094 or equivalent practical experience.<br><br><\/li><\/ul>Technical Skills<br><br><ul><li>Strong understanding of HTML5, CSS3, and JavaScript.<\/li><li>Familiarity with responsive and mobile-first development principles.<\/li><li>Basic knowledge of front-end frameworks or libraries such as React or Vue is a plus.<\/li><li>Experience with WordPress or similar CMS platforms is preferred.<\/li><li>Understanding of SEO-friendly front-end practices.<br><br><\/li><\/ul>Tools &amp; Technologies<br><br><ul><li>Familiarity with version control systems such as Git.<\/li><li>Experience working with design collaboration tools like Figma or Adobe XD.<\/li><li>Basic understanding of performance optimization and browser compatibility.<br><br><\/li><\/ul>Soft Skills<br><br><ul><li>Strong attention to detail and problem-solving abilities.<\/li><li>Good communication skills and ability to collaborate in a remote team environment.<\/li><li>Positive attitude toward learning, feedback, and professional growth.<\/li><li>Strong time management and organizational skills.<br><br><\/li><\/ul><strong>Preferred Qualifications<br><br><\/strong><ul><li>Experience with Tailwind CSS, Bootstrap, or similar CSS frameworks.<\/li><li>Basic understanding of accessibility standards (WCAG).<\/li><li>Exposure to healthcare, medical, or regulated industries is a plus.<\/li><li>Familiarity with JavaScript tooling and front-end workflows.<\/li><li>Fluent English communication skills; Arabic is a strong advantage.<br><br><\/li><\/ul>Why Join PulseMediaNL?<br><br>Competitive Compensation<br><br><ul><li>Competitive salary based on experience and skills.<\/li><li>Paid holidays and time off based on your country of residence.<br><br><\/li><\/ul>Professional Growth<br><br><ul><li>Mentorship from experienced developers and designers.<\/li><li>Opportunities to grow into mid-level front-end or full-stack development roles.<\/li><li>Hands-on experience with international healthcare and digital marketing projects.<br><br><\/li><\/ul>Fully Remote Environment<br><br><ul><li>Work remotely from anywhere in the MENA region.<\/li><li>Flexible working hours that support work-life balance.<\/li><li>Collaborative remote-first culture with modern tools and workflows.<br><br><\/li><\/ul>Supportive &amp; Innovative Culture<br><br><ul><li>Join a creative and forward-thinking team that values innovation, quality, and collaboration.<\/li><li>Work in an environment that encourages continuous learning and professional development.<br><br><\/li><\/ul>Meaningful Work<br><br><ul><li>Help build digital solutions that positively impact healthcare and wellness industries across local and global markets.<br><br><\/li><\/ul>How to Apply<br><br>If you\u00e2\u0080\u0099re a motivated Junior Front-End Developer based in the MENA region and excited to grow your career within a healthcare-focused digital agency, we\u00e2\u0080\u0099d love to hear from you.<br><br>Please submit your resume and portfolio (if available).<br><br>We are an equal opportunity employer. We welcome applicants from all backgrounds and value diverse perspectives and experiences.<br\/><br\/>Please mention the word **FUTURISTIC** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"\u00d8\u00a7\u00d9\u0084\u00d9\u0085\u00d8\u00af\u00d9\u008a\u00d9\u0086\u00d8\u00a9, \u00d8\u00a7\u00d9\u0084\u00d9\u0085\u00d8\u00af\u00d9\u008a\u00d9\u0086\u00d8\u00a9 \u00d8\u00a7\u00d9\u0084\u00d9\u0085\u00d8\u00af\u00d9\u008a\u00d9\u0086\u00d8\u00a9 \u00d8\u00a7\u00d9\u0084\u00d8\u00b3\u00d8\u00b9\u00d9\u0088\u00d8\u00af\u00d9\u008a\u00d8\u00a9","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-junior-front-end-developer-pulsemedia-apac-1132224","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-junior-front-end-developer-pulsemedia-apac-1132224"},{"slug":"remote-junior-front-end-developer-pulsemedia-apac-1132225","id":"1132225","epoch":1779494400,"date":"2026-05-23T00:00:00+00:00","company":"PULSEMEDIA (APAC)","company_logo":"","position":"Junior Front End Developer","tags":["analyst","technical","customer support","marketing","accounting","finance","education","exec","excel","legal","virtual assistant","video","microsoft","ops","saas","cloud","sales","recruiter","data entry","admin","front end","dev","design","react","wordpress","full stack","testing","web dev","javascript","css","git","seo","mobile","content writing","senior","junior","sys admin","medical","engineer","digital nomad","writer","travel","speech","ecommerce","biotech"],"description":"This role is perfect for a motivated and creative developer who is passionate about building exceptional digital experiences and eager to grow in a fast-paced, healthcare-focused environment. You\u00e2\u0080\u0099ll collaborate closely with designers, marketers, and developers to create high-quality web solutions for healthcare and medical clients.<br><br>If you enjoy front-end development, modern web technologies, and turning ideas into engaging user experiences, we\u00e2\u0080\u0099d love to hear from you.<br><br>Key Responsibilities<br><br>Front-End Development<br><br><ul><li>Build and maintain responsive, user-friendly websites and interfaces for healthcare and medical clients.<\/li><li>Convert UI\/UX designs into clean, scalable, and reusable front-end code.<\/li><li>Support the development of landing pages, websites, and digital marketing assets.<br><br><\/li><\/ul>Collaboration &amp; Teamwork<br><br><ul><li>Work closely with designers, marketers, and project managers to deliver seamless user experiences.<\/li><li>Assist with implementing front-end improvements related to SEO, CRO, and website performance.<br><br><\/li><\/ul>Website Optimization<br><br><ul><li>Optimize websites for speed, responsiveness, and cross-browser compatibility.<\/li><li>Ensure websites function smoothly across desktop, tablet, and mobile devices.<\/li><li>Follow accessibility and usability best practices.<br><br><\/li><\/ul>CMS &amp; Website Maintenance<br><br><ul><li>Maintain and update websites built on CMS platforms such as WordPress.<\/li><li>Implement content updates, layouts, and page templates based on client and internal requirements.<br><br><\/li><\/ul>Quality Assurance &amp; Debugging<br><br><ul><li>Identify and resolve front-end bugs and UI inconsistencies.<\/li><li>Test websites and features across multiple browsers and devices to ensure reliability.<br><br><\/li><\/ul>Learning &amp; Growth<br><br><ul><li>Stay current with modern front-end technologies, frameworks, and industry best practices.<\/li><li>Participate in code reviews and actively learn from senior developers and team feedback.<br><br><\/li><\/ul><strong>Experience<br><br><\/strong>Required Qualifications<br><br><ul><li>0\u00e2\u0080\u00932 years of front-end development experience (internships, freelance work, and personal projects are welcome).<\/li><li>Experience building real-world websites or web applications is a plus.<br><br><\/li><\/ul>Education<br><br><ul><li>Bachelor\u00e2\u0080\u0099s degree in Computer Science, Software Engineering, Web Development, or a related field \u00e2\u0080\u0094 or equivalent practical experience.<br><br><\/li><\/ul>Technical Skills<br><br><ul><li>Strong understanding of HTML5, CSS3, and JavaScript.<\/li><li>Familiarity with responsive and mobile-first development principles.<\/li><li>Basic knowledge of front-end frameworks or libraries such as React or Vue is a plus.<\/li><li>Experience with WordPress or similar CMS platforms is preferred.<\/li><li>Understanding of SEO-friendly front-end practices.<br><br><\/li><\/ul>Tools &amp; Technologies<br><br><ul><li>Familiarity with version control systems such as Git.<\/li><li>Experience working with design collaboration tools like Figma or Adobe XD.<\/li><li>Basic understanding of performance optimization and browser compatibility.<br><br><\/li><\/ul>Soft Skills<br><br><ul><li>Strong attention to detail and problem-solving abilities.<\/li><li>Good communication skills and ability to collaborate in a remote team environment.<\/li><li>Positive attitude toward learning, feedback, and professional growth.<\/li><li>Strong time management and organizational skills.<br><br><\/li><\/ul><strong>Preferred Qualifications<br><br><\/strong><ul><li>Experience with Tailwind CSS, Bootstrap, or similar CSS frameworks.<\/li><li>Basic understanding of accessibility standards (WCAG).<\/li><li>Exposure to healthcare, medical, or regulated industries is a plus.<\/li><li>Familiarity with JavaScript tooling and front-end workflows.<\/li><li>Fluent English communication skills; Arabic is a strong advantage.<br><br><\/li><\/ul>Why Join PulseMediaNL?<br><br>Competitive Compensation<br><br><ul><li>Competitive salary based on experience and skills.<\/li><li>Paid holidays and time off based on your country of residence.<br><br><\/li><\/ul>Professional Growth<br><br><ul><li>Mentorship from experienced developers and designers.<\/li><li>Opportunities to grow into mid-level front-end or full-stack development roles.<\/li><li>Hands-on experience with international healthcare and digital marketing projects.<br><br><\/li><\/ul>Fully Remote Environment<br><br><ul><li>Work remotely from anywhere in the MENA region.<\/li><li>Flexible working hours that support work-life balance.<\/li><li>Collaborative remote-first culture with modern tools and workflows.<br><br><\/li><\/ul>Supportive &amp; Innovative Culture<br><br><ul><li>Join a creative and forward-thinking team that values innovation, quality, and collaboration.<\/li><li>Work in an environment that encourages continuous learning and professional development.<br><br><\/li><\/ul>Meaningful Work<br><br><ul><li>Help build digital solutions that positively impact healthcare and wellness industries across local and global markets.<br><br><\/li><\/ul>How to Apply<br><br>If you\u00e2\u0080\u0099re a motivated Junior Front-End Developer based in the MENA region and excited to grow your career within a healthcare-focused digital agency, we\u00e2\u0080\u0099d love to hear from you.<br><br>Please submit your resume and portfolio (if available).<br><br>We are an equal opportunity employer. We welcome applicants from all backgrounds and value diverse perspectives and experiences.<br\/><br\/>Please mention the word **COMMENDABLE** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"\u00d8\u00b9\u00d8\u00ac\u00d9\u0085\u00d8\u00a7\u00d9\u0086, \u00d8\u00a5\u00d9\u0085\u00d8\u00a7\u00d8\u00b1\u00d8\u00a9 \u00d8\u00b9\u00d8\u00ac\u00d9\u0085\u00d8\u00a7\u00d9\u0086 \u00d8\u00b9\u00d8\u00ac\u00d9\u0085\u00d8\u00a7\u00d9\u0086 \u00d8\u00a7\u00d9\u0084\u00d8\u00a5\u00d9\u0085\u00d8\u00a7\u00d8\u00b1\u00d8\u00a7\u00d8\u00aa \u00d8\u00a7\u00d9\u0084\u00d8\u00b9\u00d8\u00b1\u00d8\u00a8\u00d9\u008a\u00d8\u00a9 \u00d8\u00a7\u00d9\u0084\u00d9\u0085\u00d8\u00aa\u00d8\u00ad\u00d8\u00af\u00d8\u00a9","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-junior-front-end-developer-pulsemedia-apac-1132225","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-junior-front-end-developer-pulsemedia-apac-1132225"},{"slug":"remote-genetic-counseling-assistant-myome-1131860","id":"1131860","epoch":1779482104,"date":"2026-05-22T20:35:04+00:00","company":"MyOme","company_logo":"","position":"Genetic Counseling Assistant","tags":["assistant","admin","healthcare","biotech","medical","coordinator"],"description":"MyOme's mission is to provide clinically actionable genetic information to patients throughout their lives. We combine clinical-grade whole genome sequencing, advanced AI methods for genome interpretation, and seamless digital tools for doctors and patients to order and access results. Our team is composed of seasoned entrepreneurs, scientists, and operators, and we're backed by top-tier investors.<br><br><strong>Position Overview:<br><br><\/strong>We are seeking a detail-oriented Genetic Counseling Assistant to support the administrative and operational needs of the Clinical Affairs team. This role is ideal for someone interested in genetics and healthcare who wants to gain exposure to the clinical side of genetic testing while providing essential logistical and administrative support.<br><br><strong>What You'll Do:<br><br><\/strong><ul><li>Assist with tracking genetic testing orders and ensuring timely processing.<\/li><li>Support the organization and management of clinical documentation and provider communications.<\/li><li>Help maintain internal databases, spreadsheets, and records related to genetic testing workflows.<\/li><li>Collaborate with genetic counselors and other team members to ensure smooth day-to-day operations.<\/li><li>Help coordinate participant-facing logistics for clinical studies, including aspects of engagement and retention.<br><br><\/li><\/ul><strong>What You'll Ne<\/strong><strong>ed:<br><br><\/strong><ul><li>Bachelor's degree in a healthcare, biology, genetics, or related field<\/li><li>Strong organizational skills and attention to detail.<\/li><li>Excellent written and verbal communication abilities.<\/li><li>Comfortable working with digital tools, databases, and spreadsheets.<\/li><li>Interest in genetics, genetic counseling, or healthcare preferred but not required.<br><br><\/li><\/ul><strong>Location, Compensation, and Benefits:<br><br><\/strong><ul><li><strong>Location: <\/strong>Remote in the US<\/li><li><strong>Compensation:<\/strong> Annual base salary range is $60,000 - $75,000, based on experience. <br><br><\/li><\/ul>San Francisco Bay Area pay range<br><br>$60,000\u00e2\u0080\u0094$75,000 USD<br><br><strong>Benefits:<br><br><\/strong><ul><li>Comprehensive healthcare coverage (Health, Dental, and Vision)<\/li><li>401K<\/li><li>Unlimited PTO<\/li><li>Professional development opportunities<\/li><li>Company-sponsored off-sites and team meals during in-person meetings<\/li><li>Direct access to company leadership and the opportunity for career growth<br><br><\/li><\/ul><strong>Diversity, Inclusion, and Equal Opportunity:<br><br><\/strong>MyOme values diversity in all forms. We believe that diverse perspectives drive better science and better patient outcomes. We are an Equal Opportunity Employer committed to creating an inclusive workplace that empowers every individual.<br><br><strong>Why Work at MyOme?<br><br><\/strong><strong>Join us if you:<br><br><\/strong><ul><li>Want to make an impact at the intersection of healthcare and technology, changing the way people engage with their health at the genetic level<\/li><li>Enjoy rolling up your sleeves, taking initiative, and being empowered to lead<\/li><li>Value humility, transparency, and collaborative problem-solving<\/li><li>Thrive in fast-moving, dynamic environments with smart, driven teammates<\/li><li>Appreciate competitive compensation, meaningful equity, and excellent benefits<br><br><\/li><\/ul>Learn More: myome.com<br\/><br\/>Please mention the word **SURMOUNT** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Durham, Durham, North Carolina, United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-genetic-counseling-assistant-myome-1131860","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-genetic-counseling-assistant-myome-1131860"},{"slug":"remote-associate-placements-upgrad-1132226","id":"1132226","epoch":1779455587,"date":"2026-05-22T13:13:07+00:00","company":"upGrad","company_logo":"","position":"Associate Placements","tags":["analyst","technical","customer support","marketing","accounting","finance","education","exec","excel","legal","virtual assistant","video","microsoft","ops","saas","cloud","sales","recruiter","data entry","admin","front end","dev","design","react","wordpress","full stack","testing","web dev","javascript","css","git","seo","mobile","content writing","senior","junior","sys admin","medical","engineer","digital nomad","writer","travel","speech","ecommerce","biotech","hr"],"description":"<p><strong>upGrad Private Limited - www.upgrad.com<\/strong><\/p><p><br><\/p><p><strong>About Us \u00e2\u0080\u0093<\/strong><\/p><p>upGrad is an online education platform building the careers of tomorrow by offering the most industry-relevant programs in an immersive learning experience. Our mission is to create a new digital-first learning experience to deliver tangible career impact to individuals at scale. upGrad currently offers programs in Data Science, Machine Learning, Product Management, Digital Marketing, and Entrepreneurship, etc. upGrad is looking for people passionate about management and education to help design learning programs for working professionals to stay sharp and stay relevant and help build the careers of tomorrow.<\/p><p><br><\/p><p><strong>Designation \u00e2\u0080\u0093<\/strong> Placements Associate<\/p><p><strong>Work Mode \u00e2\u0080\u0093<\/strong> Remote<\/p><p><br><\/p><p><strong>About the Role \u00e2\u0080\u0093<\/strong><\/p><p>upGrad is seeking <strong>enthusiastic and motivated experienced HR Professionals <\/strong>to join as <strong>Tech Placement Associates<\/strong>\/<strong>Recruiter<\/strong>. The role focuses on supporting the placement and career development of technology graduates by coordinating with hiring partners and assisting candidates in preparing for technical job opportunities.<\/p><p><br><\/p><p><strong>Key Responsibilities \u00e2\u0080\u0093<\/strong><\/p><ol><li>Manage end-to-end recruitment process for technical roles (Such as Data Engineer, Data Analyst, GEN-AI, Business Analyst etc)<\/li><li>Source candidates through database as per skills required.<\/li><li>Screen resumes and conduct initial HR interviews.<\/li><li>Assist candidates with interview preparation and job readiness<\/li><li>Track candidate progress and placement outcomes<\/li><li>Coordinate technical interviews with hiring managers and follow up on feedback.<\/li><li>Maintain candidate pipeline and update ATS regularly.<\/li><li>Build and maintain a strong talent pool for current and future hiring needs.<\/li><li>Ensure a positive candidate experience throughout the hiring process.<\/li><li>Handling key accounts, escalations, coordinating interviews.<\/li><li>Work closely with hiring managers to understand job requirements and team needs<\/li><\/ol><p><br><\/p><p><strong>Eligibility Criteria<\/strong><\/p><ul><li>Minimum 1 year experience in Tech recruitment <\/li><li>Preferably BE \/ B. Tech graduates or MBA in HR <\/li><li>Strong interest in technology and career development initiatives<\/li><li>Basic understanding of technical roles and skills like Phyton, SQL, Gen AI<\/li><li>Strong communication skills and interpersonal skills.<\/li><\/ul><br\/><br\/>Please mention the word **ADORER** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Bengaluru, Bengaluru, Karnataka, India","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-placements-upgrad-1132226","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-placements-upgrad-1132226"},{"slug":"remote-manager-model-audit-gridlines-1132227","id":"1132227","epoch":1779086089,"date":"2026-05-18T06:34:49+00:00","company":"Gridlines","company_logo":"","position":"Manager Model Audit","tags":["analyst","technical","customer support","marketing","accounting","finance","education","exec","excel","legal","virtual assistant","video","microsoft","ops","saas","cloud","sales","recruiter","data entry","admin","front end","dev","design","react","wordpress","full stack","testing","web dev","javascript","css","git","seo","mobile","content writing","senior","junior","sys admin","medical","engineer","digital nomad","writer","travel","speech","ecommerce","biotech","hr","consulting"],"description":"<strong>Company: Gridlines<br><br><\/strong>Gridlines is a rapidly growing financial modelling consultancy practice. We are transforming the world of financial modelling, helping our clients to make<br><br>complex financial decisions quickly and with confidence.<br><br>We love to work with exciting clients that are making a big impact on the world around us, helping to tackle some of the world's greatest challenges.<br><br>We plan to continue our rapid expansion and are looking for the brightest and best talent to join us on this journey.<br><br><strong> Role:<br><br><\/strong>We are seeking an experienced model audit professional that is passionate about financial modelling and driven by growth.<br><br>You will work with a team of modelling professionals to analyse and review complex financial models, ensuring they are robust and reliable.<br><br><strong>Requirements<br><br><\/strong><strong>Operations:<br><br><\/strong><ul><li> Managing a portfolio of active assignments<\/li><li> Lead model audit assignments, ensuring models are arithmetically and commercially correct<\/li><li> Use a combination of software checks and parallel model development to identify modelling errors<\/li><li> Review and interpret commercial documentation and ensure it is reflected accurately in the financial model<\/li><li> Take ownership of specific assignments and projects, demonstrating initiative and dedication to achieving high-quality outcomes<\/li><li> Contribute to the development and enhancement of our financial modelling methodologies and tools, driving continuous improvement and innovation<\/li><li> Prepare comprehensive model documentation detailing assumptions, methodologies, and results<\/li><li> Maintain meticulous records of modelling processes and methodologies to uphold our high standards and ensure consistency<\/li><li> Lead in developing project plans, timelines, and resource allocation to ensure efficient and effective project delivery<br><br><\/li><\/ul><strong>People:<br><br><\/strong><ul><li> Lead a team of model audit professionals<\/li><li> Train, motivate and manage junior team members on assignments<\/li><li> Collaborate closely with team members, learning and contributing to assignments<\/li><li> Communicate model findings and insights effectively to clients and internal teams<\/li><li> Simplify complex financial model issues to make them understandable for non-technical stakeholders<br><br><\/li><\/ul><strong>Growth:<br><br><\/strong><ul><li> Supporting in the business development and growth ambitions of a key sector of the business<\/li><li> Lead in the development of client pitches<\/li><li> Lead client calls and build client relationships<br><br><\/li><\/ul><strong>Key Skills And Qualifications<br><br><\/strong><ul><li> We hire exceptional individuals who can demonstrate our core values of Drive, Innovation, Collaboration and Excellence. <\/li><li>[4-6] years of relevent experience in a financial role within a recognized advisory practice or large corporate setting<\/li><li> A good appreciation of accounting concepts, an accounting qualification beneficial<\/li><li> An in-depth understanding of Project Finance concepts <\/li><li>Strong analytical skills with proven experience in building and operating financial models using Excel<\/li><li> Degree qualified in a numerate discipline, with a postgraduate qualification in accounting or finance beneficial<\/li><li> Experience with the FAST financial modeling standard is desirable<\/li><li> Excellent written and verbal communication skills<\/li><li> Ability to work independently and as part of a remote team<br><br><\/li><\/ul><strong>Benefits<br><br><\/strong>A competitive base salary with flexible working arrangements, including a mixture of office-based, working from home, and working on client sites.<br><br>Significant opportunities for professional growth and development as we expand.<br><br>Access to cutting-edge financial modelling tools and resources.<br><br>Collaborative and supportive team culture<br\/><br\/>Please mention the word **SUPPORTED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Gurugram, Gurugram, Haryana, India","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-manager-model-audit-gridlines-1132227","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-manager-model-audit-gridlines-1132227"},{"slug":"remote-senior-manager-biostatistician-consultant-us-clinchoice-1131597","id":"1131597","epoch":1778803223,"date":"2026-05-15T00:00:23+00:00","company":"ClinChoice","company_logo":"","position":"Senior Manager Biostatistician Consultant US","tags":["senior","manager","analyst","consulting","stats","biotech","healthcare","medical"],"description":"Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it\u00e2\u0080\u0099s the best of both worlds\u00e2\u0080\u00a6.\n\nClinChoice is searching for an Senior Manager Biostatistician Consultant to join one of our clients.\n\nClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client\u00e2\u0080\u0099s counterparts.  \n\nJob Duties\n\nThis position is responsible for working with study team members and the project statistician to contribute to design of early\/late-stage protocols across multiple therapeutic areas, help draft protocols or amendments, develop and write statistical analysis plans, and perform statistical analyses for interim and final reports to be submitted to regulatory agencies.\n\nThe position will also support submission activities, including design, analysis and reporting of integrated summaries for safety and efficacy.<br\/><br\/>Please mention the word **HOMAGE** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"United States","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-manager-biostatistician-consultant-us-clinchoice-1131597","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-manager-biostatistician-consultant-us-clinchoice-1131597"},{"slug":"remote-clinical-marketing-director-genomenon-1131562","id":"1131562","epoch":1778601619,"date":"2026-05-12T16:00:19+00:00","company":"Genomenon","company_logo":"","position":"Clinical Marketing Director","tags":["marketing","director","healthcare","medical","ai","biotech"],"description":"Our Company\n\nGenomenon is an AI-driven genetic intelligence company on a mission to save and improve lives by making biomedical information actionable. Rare diseases and cancer affect more than 30 million people in the U.S. alone and hundreds of millions globally, yet most patients still face long diagnostic journeys and limited treatment options. Our goal is clear and ambitious: to deliver the information that shapes diagnosis and treatment for every rare disease and cancer patient.\n\nWe sit at the intersection of AI, genomics, and real world evidence. Genomenon transforms the global scientific literature into a literature derived, real world evidence (RWE) engine for precision medicine\u00e2\u0080\u0094combining large-scale AI with expert human curation to deliver clean, clinically actionable datasets. This approach fills critical gaps left by EHR and claims data, especially in rare disease and oncology, by showing how patients actually present, progress, and respond to therapy.\n\nWe turn vast, complex biomedical data\u00e2\u0080\u0094spanning genomics, clinical evidence, and scientific literature\u00e2\u0080\u0094into trusted intelligence that helps clinicians make better diagnostic and therapeutic decisions, and supports life sciences organizations in bringing better therapies to market faster.\n\nOur work has real, measurable impact. Genomenon\u00e2\u0080\u0099s platforms and services are used by more than 250 clinical laboratories and pharma organizations worldwide to support diagnostic interpretation, variant curation, and evidence-based decision-making across the drug development lifecycle. \n\nEach year, our technology helps inform care for tens of thousands of patients facing rare, complex, and time-sensitive conditions\u00e2\u0080\u0094reducing uncertainty and delivering answers when they matter most.\n\nWhat makes Genomen<br\/><br\/>Please mention the word **POSITIVELY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote, USA","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-clinical-marketing-director-genomenon-1131562","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-clinical-marketing-director-genomenon-1131562"},{"slug":"remote-senior-marketing-manager-cro-experience-required-precision-medicine-group-1131536","id":"1131536","epoch":1778428826,"date":"2026-05-10T16:00:26+00:00","company":"Precision Medicine Group","company_logo":"","position":"Senior Marketing Manager CRO Experience Required","tags":["senior","marketing","manager","strategy","sales","content","biotech"],"description":"Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages\u00e2\u0080\u0094from early development through approval\u00e2\u0080\u0094with embedded experience in oncology and rare disease. With over 3500 dedicated professionals and offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.\n\nWe are seeking an accomplished Senior Marketing Manager to drive strategic marketing initiatives that support our expanding Autoimmune therapeutic area business (both full-service outsourcing [FSO] and Functional Service Provider [FSP] models), and our core CRO portfolio. This role requires a highly autonomous leader with strong cross\u00e2\u0080\u0091functional collaboration skills and the ability to translate global strategy into high\u00e2\u0080\u0091impact execution.\n\nIn this position, you will shape and refine service messaging, design and deliver integrated marketing campaigns, generate qualified leads, and empower a growing sales team in achieving their targets. You will work closely with sales and operational stakeholders to elevate market awareness, strengthen our value proposition, and accelerate lead generation across key service lines.\n\nService Marketing & Content Development\nLead and own strategic planning of marketing efforts for assigned areas, specifically all therapeutic marketing for our growing Autoimmune therapeutic area, clinical FSP, and related services. Support other services within our CRO offerings as assigned\nCreate messaging frameworks relating Feature\/Advantage\/Benefit (FAB) with proof points to optimize market positioning\nWork with stakeholders (and agencies as needed) to cr<br\/><br\/>Please mention the word **PLEASED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-marketing-manager-cro-experience-required-precision-medicine-group-1131536","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-marketing-manager-cro-experience-required-precision-medicine-group-1131536"},{"slug":"remote-senior-manager-clinical-biomarker-operations-apogee-therapeutics-1131391","id":"1131391","epoch":1777507253,"date":"2026-04-30T00:00:53+00:00","company":"Apogee Therapeutics","company_logo":"","position":"Senior Manager Clinical Biomarker Operations","tags":["senior","manager","biotech","operations","medical"],"description":"<div><div><strong>About Apogee Therapeutics<\/strong><\/div>\n<div>\n<p>Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally.<\/p>\n<p>Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&amp;I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&amp;I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care.<\/p>\n<p>We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values:&nbsp;<u>C<\/u>aring,&nbsp;<u>O<\/u>riginal,&nbsp;<u>R<\/u>esilient and&nbsp;<u>E<\/u>goless and a commitment to refusing to stop at \"good enough\".<\/p>\nIf this sounds like you, keep reading!<\/div>\n<p>&nbsp;<\/p><\/div><div><div class=\"section page-centered\" data-qa=\"job-description\">\n<div><strong>Role Summary<\/strong><\/div>\n<\/div>\n<div class=\"section page-centered\" data-qa=\"closing-description\"<br\/><br\/>Please mention the word **FERVIDLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-manager-clinical-biomarker-operations-apogee-therapeutics-1131391","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-manager-clinical-biomarker-operations-apogee-therapeutics-1131391"},{"slug":"remote-automation-engineer-syner-g-1131367","id":"1131367","epoch":1777392030,"date":"2026-04-28T16:00:30+00:00","company":"Syner-G","company_logo":"","position":"Automation Engineer","tags":["engineer","engineering","biotech"],"description":"<p><strong><u>COMPANY DESCRIPTION:<\/u><\/strong>\u00c2\u00a0<\/p>\n<p>A career here is life-enhancing.<\/p>\n<p>At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery\/success. To learn more about who we are and what drives us, watch our company video <a href=\"https:\/\/www.youtube.com\/watch?v=2rUMvtncuw8\"><strong>here<\/strong><\/a>.\u00c2\u00a0<\/p>\n<p>Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner.<\/p>\n<p>Syner-G was recently honored with BioSpace's prestigious \"Best Places to Work\" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation.\u00c2\u00a0<\/p>\n<p>At Syner-G, we <br\/><br\/>Please mention the word **CONGRATULATION** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Pittsburgh","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-automation-engineer-syner-g-1131367","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-automation-engineer-syner-g-1131367"},{"slug":"remote-senior-publications-manager-oruka-therapeutics-1131350","id":"1131350","epoch":1777334425,"date":"2026-04-28T00:00:25+00:00","company":"Oruka Therapeutics","company_logo":"","position":"Senior Publications Manager","tags":["senior","manager","medical","healthcare","biotech","content writing"],"description":"<div><p><strong>About Us:<\/strong><strong>&nbsp;<\/strong><\/p>\n<p>Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit <a href=\"http:\/\/www.orukatx.com\">www.orukatx.com<\/a><\/p>\n<p>As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger.&nbsp; Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. &nbsp;<\/p><\/div><div><p><strong>Job Title: <\/strong>Senior Publications Manager &nbsp; <strong>&nbsp; &nbsp; &nbsp;&nbsp;<\/strong><\/p>\n<p><strong>Location: <\/strong>Remote&nbsp;<strong> &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;<\/strong><\/p>\n<p><strong>Role Overview: <\/strong>We are looking for a <strong>Senior Publications Manager<\/strong> to lead publication planning and execution across our clinical and scientific programs. This role will be responsible for driving high-quality, timely development of manuscripts, abstracts, posters, and related scientific communications in close partnership with internal cross-functional teams and external medical writing vendors.<\/p>\n<p>This is a highly collaborative, hands-on role for someone<br\/><br\/>Please mention the word **IMPARTIALITY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-publications-manager-oruka-therapeutics-1131350","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-publications-manager-oruka-therapeutics-1131350"},{"slug":"remote-senior-scientific-communications-manager-oruka-therapeutics-1131349","id":"1131349","epoch":1777334414,"date":"2026-04-28T00:00:14+00:00","company":"Oruka Therapeutics","company_logo":"","position":"Senior Scientific Communications Manager","tags":["senior","manager","biotech","medical","healthcare","non tech"],"description":"<div><p><strong>About Us:<\/strong><strong>&nbsp;<\/strong><\/p>\n<p>Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit <a href=\"http:\/\/www.orukatx.com\">www.orukatx.com<\/a><\/p>\n<p>As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger.&nbsp; Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. &nbsp;<\/p><\/div><div><p><strong>Job Title: <\/strong>Senior Scientific Communications Manager&nbsp;&nbsp;<strong>&nbsp; &nbsp; &nbsp;&nbsp;<\/strong><\/p>\n<p><strong>Location: <\/strong>Remote&nbsp;<strong> &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;<\/strong><\/p>\n<p><strong>Role Overview: <\/strong>We're looking for a <strong>Senior Scientific Communications Manager<\/strong> to join our growing biotech team. This is a hands-on role for someone who enjoys turning complex scientific and clinical information into clear, accurate, and useful communications for a variety of audiences.<\/p>\n<p>At a small startup, this person will wear multiple hats. You'll help shape our scientific story externally and internally, while also building and supporting core Medical Infor<br\/><br\/>Please mention the word **GLORIOUS** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-scientific-communications-manager-oruka-therapeutics-1131349","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-scientific-communications-manager-oruka-therapeutics-1131349"},{"slug":"remote-executive-director-regulatory-affairs-kyverna-therapeutics-1131189","id":"1131189","epoch":1776412843,"date":"2026-04-17T08:00:43+00:00","company":"Kyverna Therapeutics","company_logo":"","position":"Executive Director Regulatory Affairs","tags":["exec","director","biotech","legal","senior","healthcare"],"description":"<p>\n<\/p><p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what\u00e2\u0080\u0099s possible.<\/span><\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\">&nbsp;<\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><strong><span style=\"font-size: 11.0pt;\">Title:<\/span><\/strong><span style=\"font-size: 11.0pt;\">&nbsp;Executive Director, Regulatory Affairs<\/span><\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><strong><span style=\"font-size: 11.0pt;\">Location:<\/span><\/strong><span style=\"font-size: 11.0pt;\">&nbsp;Remote (West Coast hours preferred)<\/span><\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><strong><span style=\"font-size: 11.0pt;\">Reports to<\/span><\/strong><span style=\"font-size: 11.0pt;\">: SVP, Chief Regulatory Officer<\/span><\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><strong><span style=\"font-size: 11.0pt;\">&nbsp;<\/span><\/strong><\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><strong><span style=\"font-size: 11.0pt;\">Position Overview<\/span><\/strong><\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">The Executive Director, Regulatory Affairs will provide strategic and operational regulatory leadership across Kyverna's cell therapy portfolio, with a focus on commercial readiness, labeling strategy, and health authority engagement.<\/span><\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">The ideal candidate is a seasoned regulatory leader with deep experience in advanced therapies who can shape regulatory strategy from early development through approval and launch, while partnering closely with Clinical, CMC, Commercial, Market Access, and Legal teams.<\/span><\/p>\n<p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">The Executive Director will define and execute global regulatory strategy to support clinical development, registration, and commercialization of Kyverna's autoimmune cell therapies. The role requires the ability to translate scientific and clinical data into approvable, commercially viable labeling and to lead interactions with regulatory authorities, including FDA and global counterparts.<\/span><\/p>\n<p><\/p>\\n<p><\/p><p><br><\/p><b>Responsibilities<\/b><div>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">Regulatory Strategy &amp; Leadership<\/p>\n<ul style=\"margin-bottom: 0in; margin-top: 0px;\">\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Lead global regulatory strategy for Kyverna's development programs, aligning clinical, CMC, and commercial objectives from early development through post-approval lifecycle management.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Provide regulatory input to program governance, asset prioritization, and portfolio decisions, including scenario planning and risk mitigation.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Anticipate and address regulatory challenges related to cell therapy development, manufacturing, comparability, and long-term follow-up.<\/li>\n<\/ul>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">&nbsp;<\/p>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">Health Authority Engagement &amp; Negotiations<\/p>\n<ul style=\"margin-bottom: 0in; margin-top: 0px;\">\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Serve as the primary senior regulatory interface with FDA, EMA, and other global health authorities.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Lead and\/or support key regulatory meetings, including INTERACT, pre-IND, End-of-Phase, pre-BLA\/MAA, Advisory Committees, and post-marketing commitments.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Drive regulatory negotiation strategy, including benefit-risk, endpoints, comparability, and post-approval requirements.<\/li>\n<\/ul>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">&nbsp;<\/p>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">Labeling Strategy &amp; Commercial Readiness<\/p>\n<ul style=\"margin-bottom: 0in; margin-top: 0px;\">\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Own and drive labeling strategy from early development through approval, ensuring labels support commercial differentiation, patient access, and lifecycle value.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Lead development of Target Product Profiles (TPPs) and ensure alignment across Clinical, Regulatory, Commercial, and Market Access.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Partner with Commercial, Medical Affairs, and Market Access to ensure regulatory decisions support launch readiness, promotional strategy, and payer engagement.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Lead label negotiations with health authorities, balancing scientific evidence, regulatory expectations, and commercial objectives.<\/li>\n<\/ul>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">&nbsp;<\/p>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">Regulatory Submissions &amp; Execution<\/p>\n<ul style=\"margin-bottom: 0in; margin-top: 0px;\">\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Oversee and contribute to the preparation, review, and submission of INDs, CTAs, BLAs\/MAAs, briefing packages, orphan drug applications, and other regulatory filings.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Ensure submissions are high-quality, compliant, and strategically positioned.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Maintain oversight of submission timelines, dependencies, and risk management, providing clear communication to senior leadership.<\/li>\n<\/ul>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">&nbsp;<\/p>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">Cross-Functional &amp; External Collaboration<\/p>\n<ul style=\"margin-bottom: 0in; margin-top: 0px;\">\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Act as a strategic partner to Clinical Development, CMC, Research, Commercial, Legal, BD, and Alliance Management teams.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Provide regulatory due diligence and strategic input for business development, in-licensing, out-licensing, and partnership opportunities.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Oversee regulatory activities performed by CROs, consultants, and partners, ensuring quality and strategic alignment.<\/li>\n<\/ul>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">&nbsp;<\/p>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">Team Development &amp; Operational Excellence<\/p>\n<ul style=\"margin-bottom: 0in; margin-top: 0px;\">\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Lead, mentor, and scale a high-performing regulatory team, fostering accountability, development, and a culture of collaboration.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Establish and maintain regulatory policies, procedures, and infrastructure to support a growing, late-stage organization.<\/li>\n<li style=\"margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;\">Stay current on US and global regulatory intelligence and communicate key implications to stakeholders.<\/li>\n<\/ul>\n<p style=\"margin: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\">&nbsp;<\/p>\n<\/div><p><br><\/p><b>Qualifications<\/b><div>\n<ul type=\"disc\" style=\"margin-top: 0in; margin-bottom: 0in;\">\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Bachelor's degree in a scientific discipline required; advanced degree preferred.<\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">15+ years of progressive regulatory affairs experience in pharmaceutical or biotechnology, with significant advanced therapy experience.<\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Cell and\/or gene therapy experience preferred; autoimmune disease experience highly preferred.<\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Demonstrated success leading global regulatory strategies through late-stage development and\/or approvals, ideally including BLA\/MAA experience.<\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Proven experience with labeling strategy development and negotiation, with strong understanding of commercialization impacts.<\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Deep knowledge of FDA regulations, ICH guidelines, and global regulatory frameworks; EMA and ex-US experience preferred.<\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Track record of effective engagement with FDA OTP and\/or divisions overseeing autoimmune or immune-mediated diseases.<\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Strong executive communication skills with the ability to influence senior leadership and Board-facing audiences.<\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Demonstrated ability to lead and scale teams in a fast-paced, high-growth environment. Prior supervisory experience preferred. <\/span><\/li>\n<li style=\"margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">Strategic mindset with the ability to balance scientific rigor, regulatory compliance, and commercial impact.<\/span><\/li>\n<\/ul>\n<\/div><p><br><\/p><p><\/p>\\n<p>\n<\/p><p style=\"margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;\"><span style=\"font-size: 11.0pt;\">The national base salary range for this position is $270K-$300K annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on various factors that may include but are not limited to quality and length of experience, education, geographic location and alignment with market data. This position is also eligible for bonus, benefits, and participation in the company's stock plan.<\/span><\/p>\n<p><\/p><br\/><br\/>Please mention the word **MESMERIZES** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-executive-director-regulatory-affairs-kyverna-therapeutics-1131189","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-executive-director-regulatory-affairs-kyverna-therapeutics-1131189"},{"slug":"remote-director-ai-syner-g-1131155","id":"1131155","epoch":1776326421,"date":"2026-04-16T08:00:21+00:00","company":"Syner-G","company_logo":"","position":"Director AI","tags":["director","ai","biotech","consulting"],"description":"<p><strong><u>COMPANY DESCRIPTION:<\/u><\/strong>\u00c2\u00a0<\/p>\n<p>A career here is life-enhancing.<\/p>\n<p>At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery\/success. To learn more about who we are and what drives us, watch our company video <a href=\"https:\/\/www.youtube.com\/watch?v=2rUMvtncuw8\"><strong>here<\/strong><\/a>.\u00c2\u00a0<\/p>\n<p>Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner.<\/p>\n<p>Syner-G was recently honored with BioSpace's prestigious \"Best Places to Work\" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation.\u00c2\u00a0<\/p>\n<p>At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact.\u00c2\u00a0<\/p>\n<p>For more information,<br\/><br\/>Please mention the word **ENDORSES** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-director-ai-syner-g-1131155","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-director-ai-syner-g-1131155"},{"slug":"remote-regulatory-manager-senior-regulatory-manager-precision-medicine-group-1131139","id":"1131139","epoch":1776268856,"date":"2026-04-15T16:00:56+00:00","company":"Precision Medicine Group","company_logo":"","position":"Regulatory Manager Senior Regulatory Manager","tags":["manager","senior","legal","biotech","healthcare","medical","consulting"],"description":"Precision for Medicine is not your typical CRO.  At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients.  What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. We have a strong focus on Oncology and Rare Disease.\n\nPrecision for Medicine are recruiting a Regulatory Manager \/ Senior Regulatory Manager (depending on experience) to join our team.\n\nThe Regulatory Manager provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely preparation of well organized, quality regulatory submissions in compliance with applicable regulations. The Regulatory Manager coordinates and prepares regulatory documents for submission to Regulatory Authorities and\/or Ethics Committees, as applicable. \n\nEssential functions of the job include but are not limited to:\n\n\u00e2\u0080\u00a2 Provides regulatory guidance throughout the clinical development life cycle\n\u00e2\u0080\u00a2 Compile, coordinate and review applications to Regulatory Authorities including, but not limited to, CTA\/IND, ann<br\/><br\/>Please mention the word **EASES** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote, United Kingdom","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-regulatory-manager-senior-regulatory-manager-precision-medicine-group-1131139","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-regulatory-manager-senior-regulatory-manager-precision-medicine-group-1131139"},{"slug":"remote-business-development-manager-real-world-data-glooko-1131136","id":"1131136","epoch":1776268825,"date":"2026-04-15T16:00:25+00:00","company":"Glooko","company_logo":"","position":"Business Development Manager Real World Data","tags":["bus dev","manager","sales","healthcare","biotech","analytics","strategy"],"description":"<p><strong>Business Development Manager, Real-World Data<\/strong><\/p>\n<p>Glooko is focused on helping health systems address the growing challenges of glycemic safety and diabetes management across the care continuum. With the acquisition of Monarch Medical Technologies, a Glooko Company, Glooko is uniquely positioned to be the enterprise partner of choice for healthcare providers seeking to reduce glycemic risk, improve safety, and support overburdened clinical teams with coordinated expertise across both outpatient and inpatient care settings. Glooko\u00e2\u0080\u0099s comprehensive diabetes management platform supports clinical workflow optimization and improved outcomes in the outpatient setting, while EndoTool-developed by Monarch Medical Technologies-is an FDA-cleared Class II medical device that provides patient-specific insulin dosing for hospitals. Learn more at<a href=\"http:\/\/www.glooko.com\"> www.glooko.com<\/a>.<\/p>\n<p><strong>What does a Business Development Manager, Real-World Data do at Glooko?<\/strong><\/p>\n<p>You will be a primary driver of Glooko\u00e2\u0080\u0099s&nbsp;growth within the Life Sciences sector, specifically focusing on the acquisition of new business&nbsp;and the expansion of our Real-World Data (RWD) and Real-World Evidence (RWE) offerings.&nbsp;This role requires a hunter mentality to identify, prospect, and close new partnerships with&nbsp;pharmaceutical companies, biotech firms, and research institutions. You will act as a subject&nbsp;matter expert, aligning Glooko\u00e2\u0080\u0099s unique data capabilities with the strategic research and&nbsp;commercial needs of our partners to improve outcomes in diabetes and comorbid conditions.<\/p>\n<p><strong>In this role you will:<\/strong><\/p>\n<ul>\n<li>Proactively research the Life Science industry to identify prospective partners and key&nbsp;stakeholders who require RWD\/RWE solutions for clinical research and commercial&nbsp;strategy.<\/li>\n<li>Prospecting potential partners through execution of an inside sales strategy,&nbsp;incorporating cold outreach, personalized email sequences, and LinkedIn engagement<\/li>\n<li>Define and implement stakeholder mapping and account plans that strategically build a&nbsp;network of key to drive account growth and pipeline development.<\/li>\n<li>Own the full sales cycle, from identifying opportunities to building relationships with&nbsp;key stakeholders, as well as negotiation and contracting for expansion opportunities&nbsp;with current partners.<\/li>\n<li>Coll<\/ul><br\/><br\/>Please mention the word **WILLINGNESS** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-business-development-manager-real-world-data-glooko-1131136","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-business-development-manager-real-world-data-glooko-1131136"},{"slug":"remote-scientific-director-medical-affairs-iovance-biotherapeutics-1130905","id":"1130905","epoch":1774627221,"date":"2026-03-27T16:00:21+00:00","company":"Iovance Biotherapeutics","company_logo":"","position":"Scientific Director Medical Affairs","tags":["director","medical","biotech","healthcare","strategy"],"description":"Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.\n\nOverview\u00c2\u00a0\nThe Scientific Director, Medical Affairs, and will represent Iovance Medical Affairs as needed, serving as a TIL cell therapy therapeutic area expert in educational, strategic, and tactical discussions\/presentations with internal colleagues as well as external experts and investigators. Strong surgical and\/or cell therapy expertise and recent clinical experience is required as this individual will be responsible for engagement and education with external HCP stakeholders. This role requires the ability to partner effectively with surgeons and apply practical insights into tumor procurement and perioperative workflows. They will support advisory board meetings and congress scientific forum planning. They will also collaborate with cross-functional teams to ensure the alignment of medical strategies with overarching corporate objectives.\n\nEssential Functions and Responsibilities \u00c2\u00a0\u00c2\u00a0\nResponsibilities will include, but are not limited to, the following:\n\n\u00e2\u0080\u00a2 Represent Iovance Medical Affairs as a TIL cell therapy expert in both internal and external venues including the US and Global cross-functional teams, MRB, external consults, clinical sub-teams, and advisory boards \/ steering committees.\n\u00e2\u0080\u00a2 Work cross-functionally to support Commercial Quality, Market Access, Clinical Development, and the broader Med Affairs team.<br\/><br\/>Please mention the word **ALTRUISTIC** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-scientific-director-medical-affairs-iovance-biotherapeutics-1130905","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-scientific-director-medical-affairs-iovance-biotherapeutics-1130905"},{"slug":"remote-associate-director-cmc-allucent-1130899","id":"1130899","epoch":1774598447,"date":"2026-03-27T08:00:47+00:00","company":"Allucent","company_logo":"","position":"Associate Director CMC","tags":["director","consulting","healthcare","biotech","medical","strategy","lead"],"description":"<p>We are looking for an Associate Director, Chemistry Manufacturing and Controls (CMC) to join our A-team. As an Associate Director, CMC at Allucent, you are responsible for assisting clients with Chemistry Manufacturing and Control (CMC) and related pharmaceutical development activities of drug, biologic or medical device products.  The specific experience for CMC is small molecule (solid, liquid, oral, topical, injectable (sterile products), inhalation. We are mainly focused on pre-approval products. <\/p><p>Responsibilities may include analysis\/review of drug substance synthesis, pre-formulation and formulation evaluation, analysis of manufacture, scale-up and process validation, providing support of analytical methods development and validation, and evaluation of packaging and labeling components. The CMC Associate Director leads and\/or participates in Health Authority (HA) communications including correspondences, teleconferences, and meetings. The CMC Associate Director reviews, provides advice on, or authors CMC-related regulatory content for HA submissions, reports, protocols, and other scientific documents.\u00e2\u0080\u00af\u00e2\u0080\u00af\u00c2\u00a0<\/p><p><\/p><p>At Allucent\u00e2\u0084\u00a2, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.<\/p><p><\/p><p>In this role\u00c2\u00a0your key tasks will include:<\/p><ul><ul><li>Reviews and\/or writes regulatory\/scientific documents or sections thereof, with efficiency, accuracy, and independent thought\u00c2\u00a0\u00c2\u00a0<\/li><li>Contributes significantly to strategic\/CMC discussions and associated documents\/reports regarding drug, biologic, or device development\u00c2\u00a0\u00c2\u00a0<\/li><li>Guides the writing of regulatory\/scientific documents written by other project team members\u00c2\u00a0\u00c2\u00a0<\/li><li>Has advanced scientific knowledge of HA Regulatory Guidance and Regulations\u00c2\u00a0\u00c2\u00a0<\/li><li>Interacts with various HAs, including leading HA meetings and participating as a subject matter expert; assists in preparation of meeting and briefing documents, and preparing responses to inquiries\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Contributes significantly to strategic\/CMC discussions and associated documents\/reports regarding drug, biologic, or device development issues with primary emphasis on scientific aspects\u00c2\u00a0\u00c2\u00a0<\/li><li>Has advanced understanding of electronic common technical document (eCTD) format and requirements of regulatory submissions\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Prepares product development plans and\/or strategies from early development through Phase 4\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Provides strategic advice in evaluating impact and necessary filing requirements and strategies for drug product post-approval changes\/variations\u00e2\u0080\u00af\u00c2\u00a0\u00e2\u0080\u00af\u00c2\u00a0<\/li><\/ul><ul><li>Actively supports staff learning &amp; development within the company\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Provides guidance and advises Project Leads, and\/or Project Teams\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Adherence to project budgets and contracts including scope and scope changes, timeline deliverables and active management of resources\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Manages projects as a Consulting Technical Lead as assigned\u00e2\u0080\u00af\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Leads and\/or participates in meetings with clients\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Provides mentorship to team members\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Acts professionally with peers and clients, knows business etiquette\u00e2\u0080\u00af\u00c2\u00a0<\/li><\/ul><\/ul><p><\/p>\n<p>To be successful, you will possess:<\/p><ul><li>Requires a B.S., R.Ph., M.S., Ph.D., or equivalent degree, in a scientific area, and equivalent combination of relevant experience in drug, biologic, or device development\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Scientific and regulatory knowledge of drug, biologic, or device development\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Critical thinking and analytical skills, as well as strong written and verbal communication skills in English\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Strong computer skills, including SharePoint, Word, Excel, and PowerPoint\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Quality focus\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Emotional intelligence and decision-making skills\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>Innovative, creative, and practical thinking including problem-solving skills\u00e2\u0080\u00af\u00c2\u00a0<\/li><li>\u00e2\u0089\u00a5 10 years\u00e2\u0080\u0099 post-degree of directly relevant experience in drug, biologic, or device development desirable\u00c2\u00a0<\/li><li>You have relevant work experience in a CRO or relevant industry, specific experience with small molecule (solid, liquid, oral, topical, injectable (sterile products), inhalation. <\/li><li>You are hands on and able to author eCTD CMC Module 3.0 focused on pre-approval products. <\/li><\/ul>\n<p>Benefits of working at Allucent include:<\/p><ul><li>Comprehensive benefits package per location<\/li><li>Competitive salaries per location <\/li><li>Departmental Study\/Training Budget for furthering professional development <\/li><li>Flexible Working hours (within reason) <\/li><li>Opportunity for remote\/hybrid* working depending on location<\/li><li>Leadership and mentoring opportunities <\/li><li>Participation in our enriching Buddy Program as a new or existing employee<\/li><li>Internal growth opportunities and career progression <\/li><li>Financially rewarding internal employee referral program <\/li><li>Access to online soft-skills and technical training and internal platforms<\/li><li>Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects <\/li><li>Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees<\/li><\/ul><p><\/p><p>About Allucent<\/p><p>Our mission is to help bring new therapies to light. When you work at Allucent, that means applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments.<\/p><p>If you're passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow.<\/p><p><\/p><p>Apply now!<\/p><p>Ready to bring your experience to meaningful research and Allucent, apply today or reach out to Yael Kokernoot, Sr. Manager Talent Acquisition (yael.kokernoot@allucent.com) for more information. <\/p><p><\/p><p>Disclaimers:<\/p><p>*Our in-office work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.<\/p><p><\/p><p> <\/p><p>\u00e2\u0080\u009cThe Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively \u00e2\u0080\u009cAllucent\u00e2\u0080\u009d). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.\u00e2\u0080\u009d<\/p><p><\/p><p> #LI-YK1<\/p><br\/><br\/>Please mention the word **ENTERTAINING** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-director-cmc-allucent-1130899","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-director-cmc-allucent-1130899"},{"slug":"remote-commercial-associate-molecule-xyz-1130884","id":"1130884","epoch":1774512008,"date":"2026-03-26T08:00:08+00:00","company":"molecule.xyz","company_logo":"","position":"Commercial Associate","tags":["bus dev","biotech","web3","blockchain","finance","investment","sales","operations"],"description":"<p style=\"min-height:1.5em\">Molecule and BIO.xyz are building the foundation of Decentralized Science (DeSci) \u00e2\u0080\u0094 where biotech meets web3 to make scientific research community-owned, transparent, and faster to market.<\/p><p style=\"min-height:1.5em\">Molecule provides the infrastructure to turn intellectual property (IP) into programmable, on-chain assets through our IP-NFT framework and evolving protocol stack. This enables researchers, patients, and communities to fund and govern biotech projects in new, open ways.<\/p><p style=\"min-height:1.5em\"><a target=\"_blank\" rel=\"noopener noreferrer nofollow\" href=\"http:\/\/Bio.xyz\">BIO.xyz<\/a> is the coordination and economic layer of DeSci, powering BioDAOs through funding, governance, and ecosystem alignment.<\/p><p style=\"min-height:1.5em\">Together, we are creating a new model for scientific discovery \u00e2\u0080\u0094 one where breakthroughs are owned and advanced by the communities that believe in them.<\/p><p style=\"min-height:1.5em\"><\/p><h2><strong>The Role<\/strong><\/h2><p style=\"min-height:1.5em\">We\u00e2\u0080\u0099re looking for a sharp, commercially-minded operator to work directly alongside Molecule\u00e2\u0080\u0099s CEO and Commercial Team. This role sits at the centre of everything - driving BD pipeline, managing investor relationships, handling high-priority communications with enterprise pharma partners, and ensuring nothing falls through the cracks in a fast-moving organisation.<\/p><p style=\"min-height:1.5em\">Molecule\u00e2\u0080\u0099s Commercial Team runs a high volume of concurrent partnerships across pharma, biotech, academic institutions, and investors. Deals get introduced, calls happen, and then things need someone relentless to keep them moving. You\u00e2\u0080\u0099ll work closely with the CEO and our Head of Commercial to manage the pipeline, maintain investor relations across 70+ existing investors, and build the systems that make all of this scalable.<\/p><p style=\"min-height:1.5em\">This is a role for someone who can context-switch between a pharma licensing conversation and an investor update without missing a beat - and who understands why what Molecule is building matters for the future of drug development.<\/p><p style=\"min-height:1.5em\"><\/p><h2><strong>What You\u00e2\u0080\u0099ll Do<\/strong><\/h2><ul style=\"min-height:1.5em\"><li><p style=\"min-height:1.5em\">Own follow-through on BD pipeline - track active deal workstreams across enterprise, academic, and biotech partnerships, ensure nothing stalls, and surface the right opportunities to leadership at the right time<\/p><\/li><li><p style=\"min-height:1.5em\">Manage and build investor relations - maintain relationships with 70+ existing investors through regular updates, slide decks, and follow-ups, and drive new investor relationships forward alongside the CEO and Head of Commercial<\/p><\/li><li><p style=\"min-height:1.5em\">Triage enterprise, pharma, and investor correspondence with sound commercial judgement<\/p><\/li><li><p style=\"min-height:1.5em\">Coordinate and prepare for high-stakes calls and meetings across time zones, ensuring the Team walks into every conversation fully briefed<\/p><\/li><li><p style=\"min-height:1.5em\">Draft and refine investor communications, partnership proposals, and internal updates on behalf of the Commercial Team<\/p><\/li><li><p style=\"min-height:1.5em\">Build and maintain a commercial system - create structure around how BD opportunities are categorised, tracked, and reported internally (think: our own lean CRM)<\/p><\/li><li><p style=\"min-height:1.5em\">Coordinate cross-functional deal activity - many of Molecule\u00e2\u0080\u0099s BD engagements span organisations and teams; you\u00e2\u0080\u0099ll be the connective tissue that keeps everyone aligned<\/p><\/li><li><p style=\"min-height:1.5em\">Analyse the science behind partnerships - evaluate incoming opportunities with enough scientific literacy to triage what\u00e2\u0080\u0099s worth pursuing and brief leadership accordingly<\/p><\/li><li><p style=\"min-height:1.5em\">Jump on calls with partners and investors as a credible representative of Molecule when needed<\/p><\/li><\/ul><h2><strong>Who You Are<\/strong><\/h2><ul style=\"min-height:1.5em\"><li><p style=\"min-height:1.5em\">You\u00e2\u0080\u0099re commercially hungry. Whether you came from tech sales at a startup, BD at a health-tech company, or you taught yourself commercial skills alongside your academic work - you understand pipeline, follow-up, and what it takes to close<\/p><\/li><li><p style=\"min-height:1.5em\">You\u00e2\u0080\u0099re not typically corporate. We\u00e2\u0080\u0099re not looking for someone who climbed the ladder at a large pharma company. We want someone scrappy - think a biotech startup, or someone who hustled their way through a top programme and is now looking for real ownership<\/p><\/li><li><p style=\"min-height:1.5em\">You\u00e2\u0080\u0099re organised and relentless about follow-through. The biggest gap this role fills is making sure that the volume of relationships and deals Molecule generates don\u00e2\u0080\u0099t fall through the cracks<\/p><\/li><li><p style=\"min-height:1.5em\">You\u00e2\u0080\u0099re a strong communicator - equally comfortable drafting a board-level investor memo and hopping on a call with a lab partner or KOL<\/p><\/li><li><p style=\"min-height:1.5em\">You thrive in complexity and are energised by managing multiple priorities across deals, relationships, and internal coordination simultaneously<\/p><\/li><li><p style=\"min-height:1.5em\">You have global flexibility - ideally willing to spend the first several months in Berlin for onboarding and relationship-building with the core team<\/p><\/li><\/ul><h2><strong>Nice to Have<\/strong><\/h2><ul style=\"min-height:1.5em\"><li><p style=\"min-height:1.5em\">You have a have a scientific background - ideally a Master\u00e2\u0080\u0099s or PhD in life sciences, biotech, chemistry, or a related field - and you can engage credibly with researchers and pharma partners on the substance of what they do<\/p><\/li><li><p style=\"min-height:1.5em\">Familiarity with biotech IP licensing, research collaboration agreements, or venture deal structures<\/p><\/li><li><p style=\"min-height:1.5em\">Experience working across US and European markets and navigating international stakeholder relationships<\/p><\/li><li><p style=\"min-height:1.5em\">Interest in or exposure to decentralised science, Web3, or token-based funding models<\/p><\/li><li><p style=\"min-height:1.5em\">Experience building or managing a CRM or deal-tracking system from scratch<\/p><\/li><\/ul><h2><strong>Why Molecule<\/strong><\/h2><ul style=\"min-height:1.5em\"><li><p style=\"min-height:1.5em\">Exposure to enterprise pharma, institutional investors, and cutting-edge research partnerships globally<\/p><\/li><li><p style=\"min-height:1.5em\">A team that values substance over titles, speed over process, and people who\u00e2\u0080\u0099ve built their way up<\/p><\/li><li><p style=\"min-height:1.5em\">Competitive compensation including token-based upside<\/p><\/li><\/ul><p style=\"min-height:1.5em\"><\/p><p style=\"min-height:1.5em\"><em>We are an equal opportunity employer. We are committed to equality and weaving a community that values diverse perspectives and experiences and are actively seeking a diverse pool of applicants. All employment decisions are made without regard to race, colour, national origin, ancestry, sex, gender, gender identity or expression, sexual orientation, age, genetic information, religion, disability, medical condition, pregnancy, marital status, family status, veteran status, or any other characteristic protected by law.<\/em><\/p><br\/><br\/>Please mention the word **EXCELED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-commercial-associate-molecule-xyz-1130884","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-commercial-associate-molecule-xyz-1130884"},{"slug":"remote-director-product-management-orasure-technologies-inc-1130701","id":"1130701","epoch":1773100856,"date":"2026-03-10T00:00:56+00:00","company":"OraSure Technologies Inc.","company_logo":"","position":"Director Product Management","tags":["director","product manager","product","biotech","healthcare","lead","manager"],"description":"<p>OraSure Technologies Inc. (OTI)&nbsp;empowers the global community to improve health and wellness by providing access to accurate, essential information. Our ability to positively affect change is powered by the innovative tools and diagnostics we deliver to the market.&nbsp;<\/p><p><br><\/p><p>Together with its wholly owned subsidiaries, OTI&nbsp;provides its customers with end-to-end solutions.<\/p><p><br><\/p><p>It\u00e2\u0080\u0099s first-to-market, innovative products include rapid tests for the detection of antibodies to HIV and Hepatitis C (HCV) on the OraQuick\u00c2\u00ae platform; sample self-collection and stabilization products for molecular applications; and oral fluid laboratory tests for detecting various drugs of abuse.&nbsp;&nbsp;<\/p><p><br><\/p><p><b>Overview&nbsp;<\/b><\/p><p>Here at&nbsp;OTI&nbsp;our innovative sampling tools and diagnostics unlock access to accurate, essential information that advances global health and well-being. Our products include molecular sampling kits for the genome and microbiome, and rapid diagnostics for infectious disease.&nbsp;&nbsp;<\/p><p><br><\/p><p><b style=\"font-size: 16px;\">Position Overview<\/b><\/p><p><span style=\"font-size: 16px;\">At the OraSure family of companies, our innovative sample management solutions and diagnostics unlock access to accurate, essential information that advances health and well-being globally. Our products include molecular sampling kits for the genome, microbiome and proteome and rapid diagnostics for infectious diseases.<\/span><\/p><p><span style=\"font-size: 16px;\">&nbsp;<\/span><\/p><p><span style=\"font-size: 16px;\">The Director, Product Management \u00e2\u0080\u0093 Sample Management Solutions will play a key role in driving growth of the Sample Management Solutions (SMS) business within OTI, including the Genomics collection portfolio, Microbiome collection portfolio, Colli-Pee urine collection portfolio and HEMAcollect blood collection portfolio. This role will operate in a player\/coach model. The Director will have direct responsibility for driving certain product lines and innovation projects (player) and will also lead a team of high performing product management associates in managing the remainder of the portfolio and innovation programs (coach).&nbsp; <\/span><\/p><p><span style=\"font-size: 16px;\">&nbsp;<\/span><\/p><p><span style=\"font-size: 16px;\">This position will play a key role in leading 1) the development and execution of the product roadmap for the sample management portfolio, including new product introduction and product lifecycle management; 2) development and execution of the business strategy to drive commercial success of the products within the portfolio; and 3) all other aspects of on-going product support for the assigned portfolio of products. The Director will work closely with other cross-functional leaders in the execution of these responsibilities and will ensure that business projects within the SMS portfolio are executed effectively and efficiently.&nbsp;<\/span><\/p>\\n<p><\/p><p><br><\/p><b>Responsbilities<\/b><ul><li>Lead a team in developing and executing a multi-year product roadmap for the SMS business by identifying and quantifying market opportunities, developing and assessing product concepts, and driving the development and commercialization of the products.<\/li><li>Establish and execute product lifecycle management plans for each product line within the portfolio, including evolution of claims, COGS reduction, pricing analysis, SKU consolidation and product rationalization.<\/li><li>Provide strategic leadership to the cross-functional teams for product development projects. Provide input as the voice of customer through all stages of product development, and provide clear direction to the cross-functional team.<\/li><li>Maintain a prioritized list of product initiatives and work closely with cross-functional leaders to ensure support and resourcing according to the prioritization. Clearly and quantitatively justify projects by creating business cases and forecasting customer acceptance.<\/li><li>Work cross-functionally with leaders in other departments, including R&amp;D, regulatory and clinical affairs, operations, finance, downstream marketing and sales.<\/li><li>Serve as a product expert, developing a deep understanding of the products in the portfolio and their applications. <\/li><li>Gather and evaluate customer input and be the portfolio champion, ensuring product performance meets expectations while exploring ways for continuous product improvement and market adoption growth.<\/li><\/ul><div><br><\/div><div><b>Strategy and Commercial Success<\/b><\/div><ul><li>Lead the development of the SMS business growth strategy through OTI\u00e2\u0080\u0099s annual strategy playbook process.<\/li><li>Lead the team in identifying, assessing and defining new segments for marketing and sales to target, including development of positioning and key messaging and financial projections.<\/li><li>Lead market research activities to better understand customer needs and market trends. Generate new insights that lead to the identification of new product and business opportunities.<\/li><li>Cultivate and nurture relationships with Key Opinion Leaders, advocacy organizations and external collaborators to drive product awareness and adoption and to advance product initiatives.<\/li><li>Read, understand and interpret relevant scientific literature, posters and presentations and synthesize into actionable information that can be shared within the organization.<\/li><li>Work with sales leadership to ensure support for key accounts as needed to drive ultimate customer satisfaction.<\/li><li>Partner with downstream marketing leaders to support the development of effective marketing plans and marketing collateral.<\/li><li>Lead the development of the SMS Long Range Plan 5-year financial projections.<\/li><li>Regularly analyze financial metrics to assess the health of the portfolio of products. Determine trends&nbsp;<\/li><\/ul><p><br><\/p><b>Qualifications<\/b><ul><li>Bachelor\u00e2\u0080\u0099s Degree in business or science related field is required. PhD or MBA are highly desirable<\/li><li>10+ years of experience in product management or related function. Prior product management experience in the medical devices industry (particularly diagnostics) is highly desirable<\/li><li>Strong track record of leading successful new product introductions with hands-on product development experience ranging from concept through product launch<\/li><li>Significant experience identifying and quantitatively assessing business opportunities and developing business plans to support<\/li><li>Experience conducting market research studies to understand customer needs and market trends leading to identification of new product and business opportunities<\/li><li>Experience working directly with a sales team to set and meet sales targets.<\/li><li>Experience developing key opinion leader relationships and external partnerships<\/li><li>Experience managing and coaching direct reports and developing high performing associates and teams<\/li><\/ul><div><br><\/div><div><b>Knowledge, Skills &amp; Abilities<\/b><\/div><ul><li>Ambitious, self-motivated individual with the ability to lead teams in completing complex projects without significant oversight<\/li><li>Consistent delivery of high-quality work product with appropriate attention to detail&nbsp; <\/li><li>Strong understanding of product development processes from product concept to commercialization and product lifecycle management and from launch to product rationalization. Demonstrated ability to lead others through these processes. <\/li><li>Must be able to achieve results in a cross-functional team environment, exhibiting formal and informal leadership skills and strong goal \/ results orientation. <\/li><li>Ability to lead a team of high-performing individuals to meet growth objectives &amp; strategic imperatives within the program or product area<\/li><li>Proven track record developing, driving and maintaining high performing product lines and achievement of product financial targets<\/li><li>Outstanding communication skills, including written and oral communication to senior executive audiences<\/li><li>Ability to travel throughout the US\/Canada and internationally<\/li><\/ul><p><br><\/p><p><\/p>\\n<div>$129,000 - $233,000 a year<\/div>\\n<p>&nbsp;<\/p><p><span style=\"font-size: 10.5pt\">OTI encourages applications from all qualified candidates who represent the full diversity of the communities in which we operate. &nbsp;We apply a rigorous, consistent, and equitable standard to the assessment of all candidates, regardless of race, color, national origin, sex (including pregnancy), sexual orientation, gender identity, disability status, age, religion, veteran status or any other protected characteristic. We are committed to creating a diverse and inclusive environment where all employees are welcomed and belong.<\/span><\/p><p>&nbsp;<\/p><p>&nbsp;<\/p><p>What we have to offer:<\/p><p>- Tiered Medical PPO, EPO, Vision and Dental coverage&nbsp;&nbsp;<\/p><p>- Disability and Life Insurance Benefits&nbsp;&nbsp;<\/p><p>- Generous 401K plan and company-matching contributions&nbsp;&nbsp;<\/p><p>- Highly competitive paid time-off&nbsp;&nbsp;<\/p><p>- Maternity Leave and Parental Leave Coverage&nbsp;&nbsp;<\/p><p>- Employee Referral Program \u00e2\u0080\u0093 you may be eligible for a cash bonus if your referrals are hired&nbsp;&nbsp;&nbsp;<\/p><p>- Employee Assistance Program&nbsp;<\/p><p>- Employee Service Recognition&nbsp;&nbsp;<\/p><p>- Job-related Training Programs&nbsp;<\/p><p>- Ability to participate in Teams, Committees, Events and Clubs&nbsp;<\/p><p>- Depending on the role you may be eligible to work in a hybrid environment or fully remotely&nbsp;&nbsp;<\/p><p>- Free Onsite Parking&nbsp;<\/p><p><br><\/p><p><br><\/p><p>Please note, the above applies to full-time permanent positions. <\/p><p><br><\/p><p><b>Culture, People &amp; Community<\/b>&nbsp;<\/p><p><br><\/p><p>OTI recognizes that the long-term health of our business is directly connected to the health of the planet, local communities and OTI employees.&nbsp;&nbsp;<\/p><p><br><\/p><p>- LIVE IT Committee \u00e2\u0080\u0093 committed to creating an environment that embodies our values&nbsp;&nbsp;<\/p><p>- All Means U: Employee Committee on Belonging hosts various events across all company locations such as monthly book club&nbsp;and mentorship program&nbsp;<\/p><p>- Wellness Committee empowers colleagues to make critical decisions to improve and protect health&nbsp;<\/p><p>- Sustainability Committee aims to minimize impact on the environment&nbsp;<\/p><p>- Social Committee who organize and run events for both remote and onsite employees, to create connection and community&nbsp;<\/p><p><br><\/p><p>At OTI, we have a clear vision; cultivate an environment of equal employment opportunity where we do not tolerate discrimination or allow the harassment of employees or applicants on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by law with regard to any employment practices.&nbsp;&nbsp;<\/p><p><br><\/p><p>OTI aims to create and foster workplaces that reflects and contributes to the global communities in which we do business and the customers and partners we serve. This includes all communities impacted by our corporate presence. As part of this commitment, OTI and its subsidiaries will ensure employees and applicants are provided reasonable accommodation per request.&nbsp; If you require disability-related accommodation during the recruitment process, please contact Katheryn Viau at katheryn.viau@dnagenotek.com. OTI will consult with all applicants who request disability-related accommodation during the recruitment process to ensure that the accommodation provided takes into account the applicant's individual accessibility needs.&nbsp;<\/p><p>&nbsp;<\/p><p>&nbsp;&nbsp;<\/p><p>&nbsp;<\/p><br\/><br\/>Please mention the word **ASSUREDLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-director-product-management-orasure-technologies-inc-1130701","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-director-product-management-orasure-technologies-inc-1130701"},{"slug":"remote-senior-product-manager-platform-life-sciences-scileads-1130484","id":"1130484","epoch":1771632054,"date":"2026-02-21T00:00:54+00:00","company":"SciLeads","company_logo":"","position":"Senior Product Manager Platform Life Sciences","tags":["senior","product manager","saas","ai","biotech"],"description":"<p><strong>About SciLeads:&nbsp;<\/strong><\/p>\n<p>SciLeads is a fast-growing, remote-first SaaS company helping reshape how scientific companies do sales and marketing. With over 90 people across the UK, Canada, and beyond, and plans to grow to 150+ in the next two years, our culture of openness, flexibility and innovation drives everything we do.<\/p>\n<p>We\u00e2\u0080\u0099re an award winning company, and have been listed as one of Deloitte\u00e2\u0080\u0099s fastest growing tech companies for five years in a row. We are passionate about putting people first and committed to creating an outstanding employee experience as a remote working company. Come grow your career with us!<\/p>\n<p>&nbsp;<\/p>\n<p><strong>About the Role:<\/strong><\/p>\n<p>We are looking for an experienced Senior Product Manager to turn SciLeads' product strategy into clear, high-impact execution across our platform and portfolio. You will own the translation of vision into actionable roadmaps, prioritised initiatives, and measurable outcomes that drive customer value and commercial growth. This role operates in a fast-paced, scale-up environment. Success requires comfort with ambiguity, rapid context switching, high accountability, and the ability to make confident decisions without extensive structure or iteration. You will identify market opportunities, define compelling value propositions, and ensure our products remain competitive, differentiated, and aligned to customer needs. As a senior leader within the Product function, you will help shape portfolio direction, raise the bar on product practice, and ensure consistent, high-quality execution across teams.<\/p>\n<p>Working closely with Product, Engineering, Data Ops and Commercial you will lead cross-functional delivery, support key product managers, and provide strong product leadership across the team to deliver an AI-powered marke<br\/><br\/>Please mention the word **EXPERTLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-product-manager-platform-life-sciences-scileads-1130484","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-product-manager-platform-life-sciences-scileads-1130484"},{"slug":"remote-qa-document-control-specialist-apogee-therapeutics-1130421","id":"1130421","epoch":1771459438,"date":"2026-02-19T00:03:58+00:00","company":"Apogee Therapeutics","company_logo":"","position":"QA Document Control Specialist","tags":["quality assurance","biotech","admin","coordinator","operations"],"description":"<div><div><strong>About Apogee Therapeutics<\/strong><\/div>\n<div>\n<p>Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally.<\/p>\n<p>Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&amp;I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&amp;I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care.<\/p>\n<p>We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values:&nbsp;<u>C<\/u>aring,&nbsp;<u>O<\/u>riginal,&nbsp;<u>R<\/u>esilient and&nbsp;<u>E<\/u>goless and a commitment to refusing to stop at \"good enough\".<\/p>\nIf this sounds like you, keep reading!<\/div>\n<p>&nbsp;<\/p><\/div><div><div class=\"section page-centered\" data-qa=\"job-description\">\n<div><strong>Role Summary<\/strong><\/div>\n<\/div>\n<div class=\"section page-centered\" data-qa=\"closing-description\">\n<p>We are seeking a Document Control Specia<br\/><br\/>Please mention the word **PROGRESS** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-qa-document-control-specialist-apogee-therapeutics-1130421","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-qa-document-control-specialist-apogee-therapeutics-1130421"},{"slug":"remote-associate-director-program-management-adverum-biotechnologies-inc-1130377","id":"1130377","epoch":1771372990,"date":"2026-02-18T00:03:10+00:00","company":"Adverum Biotechnologies, Inc.","company_logo":"","position":"Associate Director Program Management","tags":["director","project manager","senior","biotech","medical","manager","management","operations"],"description":"<p>We are seeking an Associate Director, Clinical Program Management to support the strategic planning, execution, and delivery of clinical programs across Adverum, with a primary focus on Phase 3 studies for Ixo\u00e2\u0080\u0091vec. This role partners closely with cross\u00e2\u0080\u0091functional teams\u00e2\u0080\u0094including Clinical Operations, Clinical Development, Regulatory, Data Management, Medical, Clinical Supply and external partners\u00e2\u0080\u0094to ensure clinical trials are executed on time, within budget, and in compliance with regulatory requirements.<\/p><p><br><\/p><p>The ideal candidate brings deep experience in clinical trial and program management, strong cross\u00e2\u0080\u0091functional leadership skills, and the ability to translate complex plans into executable timelines while proactively identifying and managing risk.<\/p><p><br><\/p><p>This position is a contract opportunity, from 6mo - 12mo.  <\/p>\\n<p><\/p><p><br><\/p><b>What you'll do:<\/b><ul><li>Contribute to the implementation of the overall clinical program management strategy in collaboration with the Sr. Director, Clinical Program Management and functional leaders<\/li><li>Support clinical program management activities across Adverum, working with key functional representatives to understand study status, identify risks, and escalate issues as appropriate<\/li><li>Plan, align, communicate, and coordinate detailed and high\u00e2\u0080\u0091level cross\u00e2\u0080\u0091functional Phase 3 study timelines<\/li><li>Collaborate with cross\u00e2\u0080\u0091functional teams to ensure alignment with integrated Phase 3 timelines and overall program milestones<\/li><li>Facilitate resolution of timeline and resource discussions, balancing team capacity with study objectives and delivery expectations<\/li><li>Track Phase 3 start\u00e2\u0080\u0091up and operational activities to ensure timelines remain on track; proactively identify risks and support escalation with recommended mitigation strategies<\/li><li>Drive coordination across teams to ensure timely planning, sequencing, communication, and completion of interdependent activities<\/li><li>Maintain critical path visibility to key study and program milestones, ensuring deliverables are clearly defined and achieved<\/li><li>Apply best practices for clinical trial conduct across all aspects of study execution, partnering with Clinical QA as needed<\/li><li>Assess and communicate the impact of changes to Phase 3 study design or program strategy<\/li><li>Support cross\u00e2\u0080\u0091functional forums to monitor trial progress, risks, action items, and timeline dependencies<\/li><li>Collaborate regularly with cross\u00e2\u0080\u0091functional PMO partners to ensure alignment with non\u00e2\u0080\u0091clinical planning and deliverables<\/li><\/ul><p><br><\/p><b>About you: <\/b><ul><li>Bachelor\u00e2\u0080\u0099s degree in life sciences, healthcare, or a related field required; advanced degree (MS, PharmD, PhD) preferred<\/li><li>Typically, 8\u00e2\u0080\u009310+ years of experience in clinical program management or clinical trial operations within biotech, pharmaceutical, or CRO environments<\/li><li>Demonstrated experience supporting complex, multi\u00e2\u0080\u0091center clinical programs from initiation through close\u00e2\u0080\u0091out<\/li><li>Strong working knowledge of clinical trial regulations and guidelines (FDA, EMA, ICH\u00e2\u0080\u0091GCP)<\/li><li>Proficiency with project and program management tools (e.g., MS Project, Gantt charts, Office timeline or equivalent)<\/li><li>Proven ability to manage cross\u00e2\u0080\u0091functional timelines, risks, and dependencies in a fast\u00e2\u0080\u0091paced environment<\/li><li>Strong communication, organizational, and problem\u00e2\u0080\u0091solving skills with the ability to influence without direct authority<\/li><\/ul><p><br><\/p><p><\/p>\\n<br\/><br\/>Please mention the word **PLEASED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Redwood City, CA","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-director-program-management-adverum-biotechnologies-inc-1130377","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-director-program-management-adverum-biotechnologies-inc-1130377"},{"slug":"remote-director-cmc-program-management-kyverna-therapeutics-1130363","id":"1130363","epoch":1771372862,"date":"2026-02-18T00:01:02+00:00","company":"Kyverna Therapeutics","company_logo":"","position":"Director CMC Program Management","tags":["director","senior","biotech","management","operations","project manager"],"description":"<p><span style=\"font-size: 11pt;\">Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what\u00e2\u0080\u0099s possible.<\/span><\/p><p><span style=\"font-size: 11pt;\">&nbsp;<\/span><\/p><p>Title: Sr. Director, CMC Program Management<\/p><p>Reports to: SVP, Clinical and Development Operations <\/p><p>Location: Remote with up to 20% travel<\/p><p><br><\/p><p><b>Summary<\/b><\/p><p>The Sr. Director of CMC Program Management will support our CMC and technical operations teams by providing program and project management expertise for a candidate cell therapy, guiding activities supporting the program through late phases of drug development including activities to support product licensure. This is a cross-functional role that will integrate all CMC aspects of a cell therapy program, including Technical Development, Manufacturing, Quality, Supply Chain, CMC Regulatory, and others. <\/p>\\n<p><\/p><p><br><\/p><b>Responsibilities<\/b><ul><li>Oversee highly complex early and late phase CMC programs and high-profile partnerships critical to the success of the company.<\/li><li>Develop and manage highly complex integrated CMC program plans, identify critical path activities and ensure milestones are identified and timeline risk is managed. <\/li><li>Provide oversight and accountability for the team member responsible for managing one or more external suppliers of LVV or Cell Drug Product, ensuring effective execution and alignment with Technical Team priorities.<\/li><li>Create and leverage appropriate project management tools to focus teams, facilitate decision making, manage risk, and ensure risks are tracked and communicated clearly within teams, to external stakeholders, and TechOps and Program leadership. <\/li><li>Partner with TechOps Leadership and finance to develop and manage highly complex program budgets, perform detailed budget analysis, and guide resourcing decisions.<\/li><li>Ensure effective communication and stakeholder management at all levels of the organization, including project teams, external CDMO partners, and TechOps and Program leadership.<\/li><li>Lead the interfaces between functional areas and with external partners to ensure effective handoff and communication between functional teams both internally and with partners to execute on important program milestones.<\/li><li>Ensure on time and in full delivery of CMC activities to support all regulatory milestones including CMC deliverables for drug licensure application. Effectively communicate with project team members, program management colleagues, Senior Leadership Team, Functional Heads, and key stakeholders. <\/li><li>Help the program management team improve PM tools for project governance and program timelines, as well as the communication of program KPIs, risks, and achievements.<\/li><li>Facilitate and improve program governance with the Senior Technical Leadership Team through dashboards, agendas, and clear communication <\/li><li>Drive efficiency and prioritization by helping TechOps balance workload across program teams, strategic initiatives, and routine operations. <\/li><li>Manage one or more direct reports, with the potential for more. Mentor junior project manager(s) to ensure commitment, collaboration and professional development<\/li><li>Provides leadership to the CMC program team and functional areas to anticipate and identify sophisticated program issues, which pose a challenge to achieving strategic goals. Implements plan to resolve such issues. <\/li><li>Identifies and anticipates CMC-related risks\/constraints to timing and resources and proactively communicates\/escalates&nbsp;&nbsp;<\/li><\/ul><div><br><\/div><p><br><\/p><b>Requirements<\/b><ul><li>Bachelor\u00e2\u0080\u0099s degree and 15+ years of program or project management experience supporting drug development is required. <\/li><li>An advanced degree such as a PhD, MS, or MD and\/or formal project management certification (e.g., PMP) is preferred.<\/li><li>Program\/Project management supporting drug development is required.<\/li><li>Direct experience working with in a Technical Operations or CMC Program Management team is required. <\/li><li>Exceptional communication skills (in person and written word) and the ability to interact with a diverse group of individuals.<\/li><li>Extensive experience managing and partnering with Contract Development and Manufacturing Organizations in the Cell and Gene Therapy space. Must have experience working on the sponsor side in Cell and Gene Therapy organizations; prior experience on the supplier side is considered a strong plus.&nbsp; <\/li><li>Experience with gene or cell therapy development programs required.<\/li><li>Experience applying the principles, concepts, practices, and standards of project management for drug development.<\/li><li>The ability to understand and communicate scientific and business elements associated with Kyverna\u00e2\u0080\u0099s engineered T cell therapies is a must.<\/li><li>Strong skills in management of external stakeholders and ability to influence and guide them toward decisions and outcomes that support Kyverna\u00e2\u0080\u0099s goals.&nbsp; &nbsp;<\/li><li>Excellent interpersonal skills, ability to develop relationships with key stakeholders, good conflict management skills.<\/li><li>Proven ability to proactively identify risks and drive resolution of issues.<\/li><li>Proven track record for delivering projects on time and in full including release of product and regulatory milestones (i.e new drug and biologics licensure applications) <\/li><li>Results and detail-oriented; self-motivated, ability to work with minimal supervision.<\/li><li>Ability to perform and be adaptive in a fast-paced environment under tight deadlines.<\/li><li>Strong analytical and problem-solving capabilities.<\/li><\/ul><p><br><\/p><p><\/p>\\n<p>The national base salary range for this position is $235K-$270K annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on various factors that may include but are not limited to quality and length of experience, education, geographic location and alignment with market data.&nbsp; This position is also eligible for bonus, benefits, and participation in the company\u00e2\u0080\u0099s stock plan. <\/p><p>&nbsp;<\/p><p><br><\/p><br\/><br\/>Please mention the word **EXCELLED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-director-cmc-program-management-kyverna-therapeutics-1130363","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-director-cmc-program-management-kyverna-therapeutics-1130363"},{"slug":"remote-senior-medical-science-liaison-xenon-pharmaceuticals-1130282","id":"1130282","epoch":1771027401,"date":"2026-02-14T00:03:21+00:00","company":"Xenon Pharmaceuticals","company_logo":"","position":"Senior Medical Science Liaison","tags":["senior","medical","healthcare","biotech"],"description":"<p style=\"min-height:1.5em\"><em><strong>Who We Are:<\/strong><\/em><\/p><p style=\"min-height:1.5em\">Xenon Pharmaceuticals (<a target=\"_blank\" rel=\"noopener noreferrer nofollow\" href=\"https:\/\/www.nasdaq.com\/market-activity\/stocks\/xene\">NASDAQ:XENE<\/a>) is a neuroscience-focused biopharmaceutical company dedicated to drug discovery, clinical development, and commercialization of life-changing therapeutics for patients in need. We are looking for great people who thrive in a respectful, collaborative, inclusive, and productive culture to join the Xenon team.<\/p><p style=\"min-height:1.5em\"><em><strong>What We Do:<\/strong><\/em><\/p><p style=\"min-height:1.5em\">We are advancing an <a target=\"_blank\" rel=\"noopener noreferrer nofollow\" href=\"https:\/\/xenon-pharma.com\/pipeline\">exciting product pipeline<\/a> to address indications with high unmet medical need, including epilepsy and depression. Our Phase 3 azetukalner program represents the most advanced, clinically validated potassium channel modulator in late-stage clinical development for multiple indications. Building upon the positive results and compelling data from our Phase 2b X-TOLE study in adult patients with focal epilepsy, our Phase 3 epilepsy program includes multiple clinical trials evaluating azetukalner in patients with focal onset seizures and primary generalized tonic-clonic seizures. In November 2025, we announced the completion of patient enrollment in our Phase 3 X-TOLE2 study, and topline data are anticipated in March 2026. We also have multiple Phase 3 azetukalner clinical trials in major depressive disorder (MDD) and bipolar depression (BPD) underway, based on topline data from our Phase 2 X-NOVA clinical trial. In addition, we are proud of the leading-edge science coming out of our discovery labs, including early-stage research programs that leverage our extensive ion channel expertise and drug discovery capabilities to identify validated drug targets and develop new product candidates. We have recently initiated Phase 1 studies for our follow-on Kv7 channel opener, XEN1120, and our lead Nav1.7 development candidate, XEN1701, in pain. Backed by a strong balance sheet to support our growth plans, we continue to build a fully integrated, premier neuroscience company with strong discovery, clinical development, corporate, and commercial operations.<\/p><p style=\"min-height:1.5em\"><em><strong>About the Role: <\/strong><\/em><\/p><p style=\"min-height:1.5em\">We are seeking a <strong>Senior Medical Science Liaison (Senior MSL)<\/strong>.  This is an opportunity to join Xenon in a field-facing role to shape and advance the MSL function in support of Medical Affairs and Clinical Development teams. This role will engage external Healthcare Providers (HCPs), Key Opinion Leaders (KOLs), and patient groups to provide education on Xenon\u00e2\u0080\u0099s pipeline in epilepsy.  <\/p><p style=\"min-height:1.5em\">This position reports to the Regional Senior Director, Field Based Medicine, and the Senior MSL will be responsible for the <strong>Northwest Region<\/strong>: Northern California, Washington, Oregon, Utah, Idaho, Montana, Wyoming, and Alaska).  Preference is for the selected individual to reside in San Francisco or Seattle area.<\/p><p style=\"min-height:1.5em\">The successful candidate is a clinical or scientific professional with a passion for science and deep scientific knowledge and a proven ability to communicate complex scientific and medical information clearly.  This candidate seeks to understand the needs of healthcare providers, patients, and families, and collaborates to solve critical scientific and business challenges. <\/p><p style=\"min-height:1.5em\"><strong>RESPONSIBILITIES:<\/strong><\/p><ul style=\"min-height:1.5em\"><li><p style=\"min-height:1.5em\">Identify, develop and maintain valued and productive scientific relationships with key external stakeholders including KOLs, HCPs, payors, academic and healthcare institutions, and advocacy groups.  <\/p><\/li><li><p style=\"min-height:1.5em\">Act as a key scientific resource to communicate up-to-date medical, clinical, and scientific information about Xenon\u00e2\u0080\u0099s neurology and epilepsy products and pipeline.<\/p><\/li><li><p style=\"min-height:1.5em\">Advance Xenon\u00e2\u0080\u0099s scientific platform and medical information in alignment with corporate and medical objectives. <\/p><\/li><li><p style=\"min-height:1.5em\">Engage in projects and\/or initiatives aligned to medical strategies and objectives; adapt plans and tactics for the assigned territory.  <\/p><\/li><li><p style=\"min-height:1.5em\">Identify and report timely and relevant scientific\/clinical insights, trends, opportunities, and threats for targeted products.<\/p><\/li><li><p style=\"min-height:1.5em\">Collaborate with internal clinical development teams to enhance patient enrollment in Xenon-sponsored clinical trials.  This includes investigator identification for clinical programs in epilepsy.<\/p><\/li><li><p style=\"min-height:1.5em\">Respond to and document unsolicited requests for scientific information. <\/p><\/li><li><p style=\"min-height:1.5em\">Lead assigned national and\/or regional congress activities in accordance with Medical Affairs strategies and plans.<\/p><\/li><li><p style=\"min-height:1.5em\">Provide instruction, coaching and mentoring to new or less experienced MSLs.<\/p><\/li><li><p style=\"min-height:1.5em\">Travel domestically up to 50% of the time, including overnight travel as business needs require. International travel may be required on an ad-hoc basis.<\/p><\/li><li><p style=\"min-height:1.5em\">Act in accordance with Company policies, including, for example, the Code of Business Conduct and Ethics and ensure policies are understood and followed by direct reports, if any.<\/p><\/li><\/ul><p style=\"min-height:1.5em\"><strong>QUALIFICATIONS:<\/strong><\/p><ul style=\"min-height:1.5em\"><li><p style=\"min-height:1.5em\">Minimum of a relevant doctorate degree (i.e. M.D., PhD, PharmD, DPH, DNP).<\/p><\/li><li><p style=\"min-height:1.5em\">Minimum 5 years relevant MSL related experience required, with 8+ years strongly preferred. Experience in neurology therapeutic area or epilepsy required<\/p><\/li><li><p style=\"min-height:1.5em\">Established relationships with KOLs and knowledge of institutions in neurology; epilepsy strongly preferred.<\/p><\/li><li><p style=\"min-height:1.5em\">Clinical trial development and drug launch experience are strongly preferred.<\/p><\/li><li><p style=\"min-height:1.5em\">Able to communicate accurately, concisely, credibly, and confidently; easily understands other points of view and responds appropriately; adjusts communication according to the audience.<\/p><\/li><li><p style=\"min-height:1.5em\">Delivers reliably against goals; proven ability to work both independently and cross-functionally; demonstrates a willingness and aptitude to learn if not yet well-versed.  <\/p><\/li><li><p style=\"min-height:1.5em\">Knowledge of clinical research processes, FDA regulations, and OIG guidelines required.<\/p><\/li><\/ul><p style=\"min-height:1.5em\">Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-&amp; long-term disability, accidental death &amp; dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions.<\/p><p style=\"min-height:1.5em\">Xenon encourages time to rest and re-charge through vacation, personal days, sick days, and an end-of-year company shutdown. Xenon highly values employee development and has an expanding Training, Learning &amp; Development program, including a Tuition Assistance program for advanced degrees.<\/p><br\/><br\/>Please mention the word **FABULOUSLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","salary_min":208000,"salary_max":233800,"apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-medical-science-liaison-xenon-pharmaceuticals-1130282","logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-senior-medical-science-liaison-xenon-pharmaceuticals-1130282"},{"slug":"remote-executive-director-safety-amp-pharmacovigilance-kyverna-therapeutics-1130274","id":"1130274","epoch":1771027337,"date":"2026-02-14T00:02:17+00:00","company":"Kyverna Therapeutics","company_logo":"","position":"Executive Director Safety &amp; Pharmacovigilance","tags":["biotech","director","exec","healthcare","medical","senior","strategy"],"description":"<p>Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what\u00e2\u0080\u0099s possible.<\/p><p>&nbsp;<\/p><p>Title: Executive Director, Safety &amp; Pharmacovigilance<\/p><p>Location: Remote<\/p><p>Reports to: VP, Head of Global Safety and Pharmacovigilance<\/p><p>&nbsp;<\/p><p><b>Summary<\/b><\/p><p>The Executive Director of Safety &amp; Pharmacovigilance (PV) will play a key role in the global safety strategy and execution for the Company\u00e2\u0080\u0099s cell therapy pipeline across clinical development and post-marketing activities. This role is responsible for leading a compliant, scalable safety organization, ensuring proactive risk management, regulatory compliance, and cross-functional collaboration to support clinical and regulatory milestones.<\/p><p>The ideal candidate brings deep expertise in cell and gene therapy safety, strong regulatory acumen, and experience operating in a lean, fast-moving biotech environment.<\/p>\\n<p><\/p><p><br><\/p><b>Responsibilities<\/b><ul><li>Define and lead the global safety and pharmacovigilance strategy across all development stages.<\/li><li>Serve as the safety subject-matter expert for cell therapy programs, including novel and emerging safety risks.<\/li><li>Provide strategic safety input to clinical development plans, protocols, investigator brochures, and regulatory submissions.<\/li><li>Act as a key member of cross-functional governance and program teams.<\/li><li>Oversee all PV activities including case processing, signal detection, risk management, and aggregate reporting.<\/li><li>Ensure compliant execution of ICSR reporting, DSURs, PBRERs\/PSURs, SUSARs, and safety narratives.<\/li><li>In collaboration with other team members, maintain safety databases, vendor oversight, and PV agreements (SDEAs).<\/li><li>Lead safety surveillance activities and ongoing benefit-risk assessments.<\/li><li>Review and approve safety data, medical assessments, and regulatory safety documents.<\/li><li>Contribute to Safety Review Committees (SRCs), Data Monitoring Committees (DMCs), and internal safety governance forums.<\/li><li>Lead safety signal evaluation, escalation, and documentation. <\/li><li>Ensure compliance with global safety regulations (FDA, EMA, ICH, CIOMS, local health authorities).<\/li><li>Partner with team lead for regulatory interactions, inspections, and audits.<\/li><li>Author or oversee safety sections of INDs and BLAs, and responses to health authority inquiries.<\/li><li>Partner with team members to maintain PV SOPs, processes, and inspection readiness.<\/li><li>Lead development and lifecycle management of Risk Management Plans (RMPs) and REMS, as applicable.<\/li><li>Proactively identify and mitigate safety risks associated with cell therapy modalities.<\/li><li>Support post-marketing safety planning and launch readiness, where applicable.<\/li><li>Collaborate in the management of external vendors, CROs, and safety service providers.<\/li><li>Contribute to the operational excellence, continuous improvement, and cost-effective PV operations.<\/li><\/ul><p><br><\/p><b>Qualifications<\/b><ul><li>MD degree <\/li><li>12+ years of experience in pharmacovigilance and drug safety, with at least 5 years in a leadership role.<\/li><li>Direct experience supporting cell therapy, gene therapy, or other advanced modalities strongly preferred.<\/li><li>Experience in clinical-stage biotech; prior BLA\/MAA and\/or launch experience is a plus.<\/li><li>Demonstrated success interacting with global regulatory agencies on safety matters.<\/li><li>Strong knowledge of global PV regulations and safety standards.<\/li><li>Strategic thinker with the ability to operate hands-on in a lean organization.<\/li><li>Excellent cross-functional leadership and communication skills.<\/li><li>Proven ability to balance compliance, scientific rigor, and business priorities.<\/li><\/ul><p><br><\/p><p><\/p>\\n<p>The national base salary range for this position is $365K-$390K annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on various factors that may include but are not limited to quality and length of experience, education, geographic location and alignment with market data.&nbsp;This position is also eligible for bonus, benefits, and participation in the company\u00e2\u0080\u0099s stock plan.&nbsp;<\/p><br\/><br\/>Please mention the word **SIMPLIFIED** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-executive-director-safety-amp-pharmacovigilance-kyverna-therapeutics-1130274","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-executive-director-safety-amp-pharmacovigilance-kyverna-therapeutics-1130274"},{"slug":"remote-channel-business-manager-10x-genomics-1130248","id":"1130248","epoch":1770998432,"date":"2026-02-13T16:00:32+00:00","company":"10x Genomics","company_logo":"","position":"Channel Business Manager","tags":["manager","sales","biotech","salesforce","operations","analytics","legal","finance","training"],"description":"<p><strong>About the role:<\/strong><br>In the Channel Business Manager role, you will be responsible for executing the overall sales strategy within the non-direct sales channels.  This includes developing on-boarding and training programs for partners, establishing and monitoring performance metrics and tools, assisting in quarterly business reviews, manage partner events, collaborate with marketing regarding promotional activities and tools, managing contracts and the channel compliance program.<\/p>\n<p><strong>What you will be doing:<\/strong><\/p>\n<ul>\n<li>Effectively onboard and offboard distributors to support global expansion and growth<\/li>\n<li>Manage distributor contract renewal and amendment process<\/li>\n<li>Coordinate with 3rd party to effectively manage the distributor compliance process<\/li>\n<li>Execute internal standardize processes around current and new partnerships<\/li>\n<li>Work closely with the Legal, Finance, Customer Service, Sales Operations, Service and Support functions to leverage and develop long standing relationships with our partners<\/li>\n<li>Liaise and interact with global field teams including coordination across commercial functions to ensure strategic alignment and plan execution for continued success of the business<\/li>\n<li>Attend distributor business reviews, and other activities to support growth<\/li>\n<li>Coordinate distributor monthly call and trainings<\/li>\n<li>Key contributor to the global distributor annual sales meeting planning<\/li>\n<li>Management of the Partner Portal, distributor promotion metrics, and SFDC opportunity management system<\/li>\n<\/ul>\n<p><strong>Minimum Qualifications:<\/strong><\/p>\n<ul>\n<li>Bachelor\u00e2\u0080\u0099s Degree, or equivalent<\/li>\n<li>Multi-year experience within Life Sciences, Biotech, or Diagnostics in a global commercial capacity with a strong understanding of Academic, Pharmaceutical and Biotech customer segments<\/li>\n<li>Experience in working with distributors, contract management and analytics reporting<\/li>\n<\/ul>\n<p><strong>Preferred Skills:<\/strong><\/p>\n<ul>\n<li>Demonstrable ability to manage multiple<br\/><br\/>Please mention the word **IMMENSE** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Australia","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-channel-business-manager-10x-genomics-1130248","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-channel-business-manager-10x-genomics-1130248"},{"slug":"remote-marketing-associate-beacon-biosignals-1130212","id":"1130212","epoch":1770854604,"date":"2026-02-12T00:03:24+00:00","company":"Beacon Biosignals","company_logo":"","position":"Marketing Associate","tags":["marketing","events","biotech","content","strategy"],"description":"Beacon Biosignals is on a mission to revolutionize precision medicine for the brain. We are the leading at-home EEG platform supporting clinical development of novel therapeutics for neurological, psychiatric, and sleep disorders. Our FDA 510(k)-cleared Waveband EEG headband and AI algorithms enable quantitative biomarker discovery and implementation. Beacon's Clinico-EEG database contains EEG data from nearly 100,000 patients, and our cloud-native analytics platform powers large-scale RWD\/RWE retrospective and predictive studies. Beacon Biosignals is changing the way that patients are treated for any disorder that affects brain physiology. \n\nWe're looking for an organized, innovative marketing professional to serve as the operational engine behind our Life Sciences Marketing team. You'll be the person who makes things happen, turning strategy into action, managing the details that drive results, and building systems that help our marketing and business development teams work smarter.\n\nBeacon's robust asynchronous work practices ensure a first-class remote work experience, but we also have in-person office hubs available located in Boston, New York and Paris.\n\nWhat success looks like:\n\nEvents & Conference Strategy \n\nOwn our conference calendar end-to-end, from identifying opportunities to post-event ROI analysis \nCoordinate all event logistics including sponsorships, travel, registration, vendor relationships, and budget tracking \nDevelop pre- and post-event outreach strategies, including attendee targeting and follow-up campaigns \nManage deadlines around scientific content submissions (abstracts, posters) and social amplification around events \n\nAudience Deve<br\/><br\/>Please mention the word **SPLENDIDLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Boston, MA","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-marketing-associate-beacon-biosignals-1130212","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-marketing-associate-beacon-biosignals-1130212"},{"slug":"remote-cell-therapy-account-management-north-carolina-south-carolina-iovance-biotherapeutics-1130063","id":"1130063","epoch":1770163325,"date":"2026-02-04T00:02:05+00:00","company":"Iovance Biotherapeutics","company_logo":"","position":"Cell Therapy Account Management North Carolina South Carolina","tags":["biotech","sales","manager","medical","healthcare"],"description":"<h4>The ideal candidate will live in North Carolina or South Carolina.<\/h4>\n<h4>Overview<\/h4>\n<p>Amtagvi\u00e2\u0084\u00a2 is the best-in-class cell therapy treatment for advanced melanoma. The Cell Therapy Account Management Associate (CTAM) will be responsible for contributing to pipeline growth of Amtagvi demand by developing a referral network between community practices and academic centers; enable early patient identification and streamline referral pathways; and collaborate with internal teams to ensure scientific and operational excellence in cell therapy account management.<\/p>\n<p>To succeed in this role, you will use prior experience in a similar role within the oncology rare disease space. The ability to influence others, perform referral and education activities, building awareness and relationships. You are expected to understand account management and strategy planning. Additional competencies include knowledge of immunotherapy and solid tumor cancer, as well as the ability to launch, drive demand, pull through, and sustain the growth of Amtagvi\u00e2\u0084\u00a2.<\/p>\n<p><strong>Essential Functions and Responsibilities:<\/strong><\/p>\n<ul>\n<li>Drive Amtagvi<sup>TM<\/sup> demand and appropriate pull-through at targeted ATCs and serve as a liaison between community oncology practices and internal stakeholders to align initiatives with business and medical objectives.<\/li>\n<li>Collaborates closely with Iovance iPOD at authorized treatment centers offering commercially available Amtagvi<sup>TM<\/sup>.&nbsp;Responsible for developing and onboarding a new TIL service line at target ATCs.<\/li>\n<li>Educate site personnel on clinical and product information for Amtagvi<sup>TM<\/sup>.<\/li>\n<li>Provide knowledge around Iovance products and processes to all service line customer stakeholders.<\/li>\n<li>Collaborate with ATC Operations, to ensure Iovance Cell Therapy logistics, processes, and operations.<\/li>\n<li>Provide customer service w<br\/><br\/>Please mention the word **ENJOY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"North Carolina","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-cell-therapy-account-management-north-carolina-south-carolina-iovance-biotherapeutics-1130063","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-cell-therapy-account-management-north-carolina-south-carolina-iovance-biotherapeutics-1130063"},{"slug":"remote-regional-customer-support-specialist-natera-1129823","id":"1129823","epoch":1769482806,"date":"2026-01-27T03:00:06+00:00","company":"Natera","company_logo":"","position":"Regional Customer Support Specialist","tags":["customer support","healthcare","medical","biotech","support","admin","sales"],"description":"<p><strong>POSITION SUMMARY:<\/strong><\/p>\n<p>The Regional Customer Support Specialist, known internally as Territory Manager, supports Natera\u00e2\u0080\u0099s division and provides world class service to customers consisting of medical professionals, patients and cross functional internal and external teams. This position primarily consists of working with customers and sales representatives to ensure a smooth ordering process and quick reporting of results. Requires ability to work independently, multi-task, and use critical thinking skills to resolve issues in a timely manner.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>PRIMARY RESPONSIBILITIES<\/strong><\/p>\n<ul>\n<li>\n<p>Respond promptly to internal and external customer inquiries.<\/p>\n<\/li>\n<li>\n<p>Serve as the lead contact for accounts and Sales and document all interactions, communications, actions taken, and follow ups.<\/p>\n<\/li>\n<li>\n<p>Build rapport with accounts, patients and Sales to resolve missing information in a timely manner, ensuring TAT is met.<\/p>\n<\/li>\n<li>\n<p>Communicate delays and cancellations to customers and help facilitate redraw of samples as needed.<\/p>\n<\/li>\n<li>\n<p>Deals directly with internal and external customers via telephone and electronic channels to research and resolve escalated issues and communicate clearly and logically root cause of issue and resolution.<\/p>\n<\/li>\n<li>\n<p>Familiarity with all oncology tests performed by Natera, including samples needed, TAT to results, all required patient health information, proper completion of request forms, and required waivers.<\/p>\n<\/li>\n<li>\n<p>Special projects and other duties may be assigned to meet business needs.<\/p>\n<\/li>\n<li>\n<p>This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job.<\/p>\n<\/li>\n<li>\n<p>Must maintain a current status on Natera training requirements.<\/p>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>QUALIFICATIONS<\/strong><\/p>\n<ul>\n<li>\n<p>Two year degree and\/or 2-5 years of related experience, undergraduate degree preferred.<\/p>\n<\/li>\n<li>\n<p>Skilled specialist, completes tasks in a resourceful and efficient manner.<\/p>\n<\/li>\n<li>\n<p>Advanced professional growth education.<\/p>\n<\/li>\n<li>\n<p>Must complete training relating to HIPAA\/PHI privacy, general policies and procedure compliance training and security training as soon as possible but not later than the first 30 days of hire.<\/p>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>KNOWLEDGE, SKILLS, AND ABILITIES<\/strong><\/p>\n<ul>\n<li>\n<p>Excellence in de-escalating customer behavior.<\/p>\n<\/li>\n<li>\n<p>Excellent organizational skills and ability to balance multiple client needs and internal stakeholders.<\/p>\n<\/li>\n<li>\n<p>Problem analysis and problem solving skills.<\/p>\n<\/li>\n<li>\n<p>Adaptability to change and self-starter.<\/p>\n<\/li>\n<li>\n<p>Knowledge of customer service principles and practices.<\/p>\n<\/li>\n<li>\n<p>Experience in both phone and written customer support.<\/p>\n<\/li>\n<li>\n<p>Knowledge of administrative procedures and protocols.<\/p>\n<\/li>\n<li>\n<p>Knowledge of numer<br\/><br\/>Please mention the word **REVIVAL** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"US Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-regional-customer-support-specialist-natera-1129823","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-regional-customer-support-specialist-natera-1129823"},{"slug":"remote-regional-sales-director-bridgebio-pharma-1129811","id":"1129811","epoch":1769472281,"date":"2026-01-27T00:04:41+00:00","company":"BridgeBio Pharma","company_logo":"","position":"Regional Sales Director","tags":["director","sales","manager","biotech","healthcare","lead","exec"],"description":"<div><h3><u>Mavericks Wanted<br><\/u><\/h3>\n<p>When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on<br>&nbsp;<br>In 2015, we pioneered a \"moneyball for biotech\" approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows&nbsp;science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.&nbsp;<br>&nbsp;<br>Together we define white space, push boundaries and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask \"why not?\" and help reengineer the future of biopharma.<\/p>\n<h3><u>What You'll Do<\/u><\/h3>\n<p>We are hiring a team of Regional Sales Directors nationwide! <\/p>\n<p>The Regional Sales Director<span style=\"color: #000000;\"> is a high-impact, front-line leadership position that is critically important to BridgeBio's success. They will be a talented leader with strategic acumen, commercial capabilities, and leadership skills to build and motivate a high-performing sales team to execute product launches with sustained excellence. They will bring experience in scaling and launching successful drugs. In doing such, they will bring passion, urgency, and a get-it-done attitude to treating unmet needs in patients. Given the company's mission to serve patients, the RSD will also possess clear alignment to this ultimate mission to keep the patient front and center.<\/span><\/p>\n<h3><u>Responsibilities<\/u><\/h3>\n<ul>\n<li>\n<p>Build a performance driven and patient-focused sales force with end-to-end responsibilities from hiring to performance management<\/p>\n<\/li>\n<li>\n<p>Motivate and inspire teams from pre-launch through commercialization, including launch readiness and post-approval execution by the sales force<\/p>\n<\/li>\n<li>\n<br\/><br\/>Please mention the word **CUSHY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-regional-sales-director-bridgebio-pharma-1129811","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-regional-sales-director-bridgebio-pharma-1129811"},{"slug":"remote-robotic-sales-representative-japan-procept-biorobotics-1129803","id":"1129803","epoch":1769472217,"date":"2026-01-27T00:03:37+00:00","company":"PROCEPT BioRobotics","company_logo":"","position":"Robotic Sales Representative Japan","tags":["sales","robotics","medical","healthcare","biotech"],"description":"<p><b>Company Overview<\/b><\/p><p>Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. At PROCEPT, we put the patient first in everything we do and&nbsp;are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders. That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.<\/p><p><br><\/p><p><b>The Opportunity That Awaits You: &nbsp;&nbsp;<\/b><\/p><p>This position is responsible for selling the Aquabeam Robotic System to greenfield and existing hospitals in the defined territory and establishing Aquablation as the treatment of choice for men suffering from BPH. This is a business-critical role and as such requires a highly motivated individual focused on executing activities and exceeding sales targets. The individual will need to demonstrate the ability to build a team of advocates within each hospital, strong solution selling skills, and enough tenacity to ensure sales objectives are met on a consistent basis. &nbsp;They will need to balance between tactical implementation of programs, strategic decision making and work effectively with all external stakeholders including clinicians and administration as well as PROCEPT\u00e2\u0080\u0099s internal functional area.<\/p>\\n<p><\/p><p><br><\/p><b>What Your Day-To-Day Will Involve:<\/b><ul><li>Meet or exceed quarterly sales quota for the defined area<\/li><li>Work with the sales manager to develop a plan that outlines sales objectives tailored to the local market&nbsp;<\/li><li>Manage the complex sales process of the Aquabeam System into new and existing hospitals<\/li><li>Build clinical and administrative support through technical presentations, executive meetings and marketing events<\/li><li>Build support from surgeons and administration for Aquablation therapy<\/li><li>Identify key institutions, generate market awareness, and drive sales of the Aquabeam System within an assigned sales      territory<\/li><li>Effectively manage transition of initial sale and installation to the Aquablation sales team to drive procedural volume and      growth<\/li><li>Develop initial contact with CEO and senior hospital administrators<\/li><li>Provide monthly forecasts for defined area<\/li><li>Effectively communicate AquaBeam\u00e2\u0080\u0099s value proposition to customers<\/li><li>Build and maintain relationships with key customers and KOLs within region<\/li><li>Partner closely with Sales Management and the Marketing team to identify and prioritize customers for higher-level      corporate relationships<\/li><li>Partner with the Customer Service team to meet and exceed customer expectations<\/li><li>Ensure all required sales reporting forms are completed and submitted on time<\/li><li>Maintain records in the PROCEPT CRM system on contacts and facilities<\/li><li>Provide support in the resolution of product complaints and\/or safety issues<\/li><li>Proactively support organizational goals and objectives, policies and procedures, and FDA regulations including strict      compliance with AquaBeam\u00e2\u0080\u0099s Customer Relationship and the Sunshine Act policies<\/li><li>Maintain a professional and credible image with customers and teammates<\/li><li>Establish and maintain credentials to enter and work in hospitals and other medical facilities as required by facility      requirements<\/li><li>Manage travel and expenses per approved budget<\/li><li>Maintain trained status for, and comply with, all relevant aspects of the PROCEPT BioRobotics Quality Management System to      ensure product and support regulatory compliance<\/li><\/ul><p><br><\/p><b>The Qualifications We Need You to Possess:<\/b><ul><li>Bachelor\u00e2\u0080\u0099s degree from accredited reputable institution&nbsp;<\/li><li>A minimum of five years of experience in medical and capital sales within the Operating Room&nbsp;<\/li><li>Start-up company experience selling disruptive surgical technology&nbsp;<\/li><li>Strong local relationships within the healthcare community in specified geographic area&nbsp;<\/li><li>Leadership skills as demonstrated through past professional performance, involvement in sports, professional clubs, or associations.<\/li><li>Ability to travel 60-70% in Japan<\/li><li>Robotics Experince<\/li><\/ul><p><br><\/p><p><\/p>\\n<p><b>Understanding PROCEPT's Culture<\/b><\/p><p>At <b>PROCEPT<\/b>, we believe every person matters. Every employee, every patient, every caregiver. Because we are here to create a revolution, and we believe in doing that by innovating everywhere with pathological optimism. We believe in being humble and highly engaged in the work we do, while also working together seamlessly for a common goal. At Procept, curiosity, ingenuity and conviction in the power technology will transform the lives of our patients and providers.<\/p><p>&nbsp;<\/p><p>And this doesn\u00e2\u0080\u0099t happen by accident. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept\u00e2\u0080\u0099s history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do. It continues with our one-of-a-kind management program designed to build the best managers in the industry, where our people managers across functions come together to exchange ideas and grow, as both managers and learners, in an environment that challenges, supports and broadens.<\/p><p>&nbsp;<\/p><p>We are fueled by the opportunity to give people their lives back. And we believe that it begins with YOU! At Procept, we push beyond just finding a work\/life balance, we strive to find a work\/life blend, a professional world that you are honored and impassioned to belong to, one that you can proudly share with your family, friends, and acquaintances. <\/p><p>&nbsp;<\/p><p>An opportunity at PROCEPT BioRobotics won\u00e2\u0080\u0099t just be about finding a job. It will be an opportunity for you to join a community devoted to making a difference in this world!<\/p><p>&nbsp;<\/p><p><b>BENEFITS OF WORKING AT PROCEPT!<\/b>&nbsp;<\/p><p><b>PROCEPT\u00e2\u0080\u0099s <\/b>health and wellness benefits for employees are second to none in the industry. As an organization, one of our top priorities is to maintain the health and wellbeing of our employees and their families. We offer a comprehensive benefits package that includes full medical coverage, wellness programs, on-site gym, a 401(k) plan with employer match, short-term and long-term disability coverage, basic life insurance, wellbeing benefits, flexible or paid time off, paid parental leave, paid holidays, and many more! <\/p><p><br><\/p><p><b>EQUAL EMPLOYMENT OPPORTUNITY STATEMENT<\/b><\/p><p>PROCEPT BioRobotics is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind on the basis of race, color, national origin, religion, gender, gender identity, sexual orientation, disability, genetic information, pregnancy, age, or any other protected status set forth in federal, state, or local laws. This policy applies to all employment practices within our organization.<\/p><p>&nbsp;<\/p><p><b>PAY RANGE TRANSPARENCY<\/b><\/p><p>Procept is committed to fair and equitable compensation practices. The pay range(s) for this role represents a base salary range for non-commissionable roles or on-target earnings for commissionable roles. Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, relevant certifications and training, and specific work location. Based on the factors above, Procept utilizes the full width of the range. The total compensation package for this position may also include eligibility for annual performance bonus, equity, and the benefits listed above.<\/p><p>&nbsp;<\/p><p><b>WORK ENVIRONMENT<\/b><\/p><p>We\u00e2\u0080\u0099ll provide you training for, and ask you to maintain trained status for, and comply with, all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance. We would also ask you to understand and adhere to the PROCEPT BioRobotics Quality &amp; EHS policies.<\/p><p><br><\/p><p><b style=\"font-size: 11pt;\">PROCEPT BioRobotics \u00e2\u0080\u0093 Applicant Privacy Notice<\/b><\/p><p><span style=\"font-size: 11pt;\">When you submit an application on this site, PROCEPT BioRobotics collects the personal information you provide. This may include your name, email address, phone number, r\u00c3\u00a9sum\u00c3\u00a9 or CV, LinkedIn profile, and any optional demographic information you choose to share, such as gender or ethnicity. We use this information to review your application and assess your suitability for the role.<\/span><\/p><p><span style=\"font-size: 11pt;\">&nbsp;<\/span><\/p><p><span style=\"font-size: 11pt;\">To learn more about how we handle personal information, including your rights under applicable privacy regulations, please read our full Privacy Notice at: <\/span><b><span style=\"font-size: 11pt;\">[<\/span><\/b><a href=\"https:\/\/www.procept-biorobotics.com\/privacy-policy\"><b><span style=\"font-size: 11pt;\">Privacy Policy<\/span><\/b><\/a><b><span style=\"font-size: 11pt;\">]<\/span><\/b><span style=\"font-size: 11pt;\">.<\/span><\/p><br\/><br\/>Please mention the word **FRIENDLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Japan","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-robotic-sales-representative-japan-procept-biorobotics-1129803","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-robotic-sales-representative-japan-procept-biorobotics-1129803"},{"slug":"remote-computational-biologist-bio-1129791","id":"1129791","epoch":1769472123,"date":"2026-01-27T00:02:03+00:00","company":"BIO","company_logo":"","position":"Computational Biologist","tags":["python","ai","biotech","data science","analyst","work from home"],"description":"<p style=\"min-height:1.5em\">Bio is a decentralized science protocol that helps launch and grow AI-driven biotech research. It enables scientists to raise funds, create value from their work, and distribute that value directly to their communities. Since 2023, Bio has directed over $50m to global researchers, offering an alternative to traditional pharma funding. Backed by investors like Binance Labs, Northpond Ventures, and Animoca Brands, Bio accelerates real-world therapeutics across longevity, brain health, fertility, psychedelic science, and more.<\/p><p style=\"min-height:1.5em\"><\/p><h2><strong>The Role<\/strong><\/h2><p style=\"min-height:1.5em\">We're looking for a computational biologist to serve as the bridge between our AI systems and physical reality. We need someone who can programmatically QA the high-volume outputs of our AI before they reach the bench - catching errors that are invisible to humans but obvious in the data.<\/p><p style=\"min-height:1.5em\"><\/p><h2><strong>What You'll Do<\/strong><\/h2><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Validate AI outputs using computational methods - simulations, structural analysis, database cross-referencing<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Translate AI predictions into executable protocols for cloud labs (Emerald, Strateos) or technical specs for CROs<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Build and maintain validation pipelines that catch errors before they waste lab resources<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Manage the \"hand-off\" between digital predictions and physical experiments<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Transform JSON outputs from our agents into experimental protocols and validation workflows<\/p><p style=\"min-height:1.5em\"><\/p><h2><strong>What We're Looking For<\/strong><\/h2><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 PhD in Computational Biology, Bioinformatics, or related field preferred - or equivalent exceptional experience<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Strong proficiency in Python and\/or R for data analysis and pipeline development<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Experience with computational validation methods (molecular simulations, structural analysis, sequence analysis)<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Ability to critically evaluate biological predictions and identify potential issues<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Comfort working at the interface of software and biology<\/p><p style=\"min-height:1.5em\"><\/p><h2><strong>Nice to Have<\/strong><\/h2><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Experience with cloud lab platforms (Emerald, Strateos, or similar)<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Background working with CROs or translating computational work to wet-lab execution<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Familiarity with AI\/ML systems and their failure modes<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Experience red-teaming or adversarially testing scientific predictions<\/p><p style=\"min-height:1.5em\"><\/p><h2><strong>Why Bio<\/strong><\/h2><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Work at the cutting edge of AI-driven biology<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Fully remote - work from anywhere<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Small team where your expertise directly shapes our science<\/p><p style=\"min-height:1.5em\">\u00e2\u0080\u00a2 Competitive compensation with token\/equity component<\/p><br\/><br\/>Please mention the word **AMAZEMENT** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-computational-biologist-bio-1129791","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-computational-biologist-bio-1129791"},{"slug":"remote-associate-director-manufacturing-science-and-technology-apogee-therapeutics-1129518","id":"1129518","epoch":1768172435,"date":"2026-01-11T23:00:35+00:00","company":"Apogee Therapeutics","company_logo":"","position":"Associate Director Manufacturing Science and Technology","tags":["biotech","director","operations","senior","technical"],"description":"<p>&nbsp;<\/p>\n<div><strong>About Apogee Therapeutics<\/strong><\/div>\n<div>Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally.<\/div>\n<div>Apogee Therapeutics,&nbsp;Inc.&nbsp;is a biotechnology company&nbsp;seeking to develop differentiated biologics for the treatment of atopic dermatitis, chronic obstructive pulmonary disease and other inflammatory and immunology indications with high unmet need.&nbsp;Our antibody programs are designed to potentially overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties.&nbsp;We seek to reshape the current standard of care for inflammatory and immune diseases because we believe people living with these diseases deserve the best possible treatment, and we refuse to stop at \u00e2\u0080\u009cgood enough.\u00e2\u0080\u009d<\/div>\n<div>We are a fast-paced company committed to building an exceptional company culture, founded on our C.O.R.E. values: <u>C<\/u>aring, <u>O<\/u>riginal, <u>R<\/u>esilient and <u>E<\/u>goless.&nbsp;<\/div>\n<div>If this sounds like you, keep reading!<\/div>\n<p>&nbsp;<\/p><\/div>\n<div><div class=\"section page-centered\" data-qa=\"job-description\">\n<div><strong>Role Summary<\/strong><\/div>\n<\/div>\n<div class=\"section page-centered\" data-qa=\"closing-description\">\n<p>We are seeking a dynamic and experienced MSAT Associate Director to support late-stage development through launch\/commercialization activities. Central to success will be engaging with CDMO(s) to deliver processes that enable robust production of Drug Substan<br\/><br\/>Please mention the word **CONVENIENCE** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-director-manufacturing-science-and-technology-apogee-therapeutics-1129518","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-associate-director-manufacturing-science-and-technology-apogee-therapeutics-1129518"},{"slug":"remote-lead-omics-workflow-engineer-axle-1129445","id":"1129445","epoch":1767657748,"date":"2026-01-06T00:02:28+00:00","company":"Axle","company_logo":"","position":"Lead Omics Workflow Engineer","tags":["lead","engineer","biotech","senior","data science"],"description":"(ID: 2026-1406)\n\nAxle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).\n\nBenefits We Offer:\n- 100% Medical, Dental & Vision Coverage for Employees\n- Paid Time Off and Paid Holidays\n- 401K match up to 5%\n- Educational Benefits for Career Growth\n- Employee Referral Bonus\n- Flexible Spending Accounts:\n  - Healthcare (FSA)\n  - Parking Reimbursement Account (PRK)\n  - Dependent Care Assistant Program (DCAP)\n  - Transportation Reimbursement Account (TRN)\n\nThe Opportunity: Your Impact<br\/><br\/>Please mention the word **EXHILARATINGLY** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-lead-omics-workflow-engineer-axle-1129445","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-lead-omics-workflow-engineer-axle-1129445"},{"slug":"remote-medical-affairs-writer-contract-kyverna-therapeutics-1129320","id":"1129320","epoch":1766448172,"date":"2025-12-23T00:02:52+00:00","company":"Kyverna Therapeutics","company_logo":"","position":"Medical Affairs Writer Contract","tags":["medical","writer","biotech","healthcare","work from home","part time"],"description":"<p>Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, <b>Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome<\/b>, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what\u00e2\u0080\u0099s possible.<\/p><p>&nbsp;<\/p><p>Kyverna is seeking a <b>Medical Communications Medical Affairs Writer (Contract)<\/b> responsible for the development, coordination, and execution of high-quality scientific publications, congress materials, and medical content that communicate clinical and translational data accurately, compliantly, and effectively. This role partners closely with Medical Affairs, Clinical Development, Biostatistics, Regulatory, and other external writers to ensure timely dissemination of data in accordance with global publication standards and company objectives.<\/p><p>This is a highly cross-functional role requiring strong scientific writing expertise, attention to detail, and the ability to manage multiple deliverables in a fast-paced clinical-stage environment.<\/p><p>&nbsp;<\/p><p><b>Title: <\/b>Medical Affairs Writer - Contract<\/p><p><b>Reports to: <\/b>Scientific Director, Medical Affairs<\/p><p><b>Location: <\/b>Remote<\/p><p><b>Duration: <\/b>12 months. 15-30 hours per week depending on workload<\/p><p><b>Hourly rate: <\/b>$90\/hr-$110\/hr<\/p>\\n<p><\/p><p><br><\/p><b>Responsibilities<\/b><ul><li>Support the development and execution of the global medical communication and publication plans aligned with Medical Affairs and clinical program objectives<\/li><li>Author, edit, and manage a range of publication and other medical communication deliverables, including:<\/li><li>\tPrimary manuscripts<\/li><li>\tReview articles<\/li><li>\tAbstracts<\/li><li>\tSlide Decks (MSL and HCP)<\/li><li>\tCongress posters and oral presentations<\/li><li>\tPlain language summaries (as applicable)<\/li><li>Ensure content is scientifically accurate, balanced, and aligned with source data<\/li><li>Translate complex clinical, preclinical, and translational data into clear, compelling scientific narratives<\/li><li>Manage internal review, approval workflows, and version control<\/li><li>Partner with Clinical Development, Biostatistics, Regulatory, Commercial (as appropriate), and external medical writers<\/li><li>Support author engagement, including coordinating feedback and revisions with key opinion leaders (KOLs)<\/li><li>Inquiry management \u00e2\u0080\u0093 Monitor the inquiry inbox and respond to patient and physician inquiries using approved templates<\/li><\/ul><p><br><\/p><b>Qualifications<\/b><ul><li>Advanced degree in a scientific or medical discipline (PhD, PharmD, MD, or MS with relevant experience)<\/li><li>10+ years of medical or scientific writing experience in publications within biotech, pharma, or medical communications<\/li><li>Demonstrated experience authoring manuscripts, abstracts, and congress materials<\/li><li>Strong understanding of clinical trial design, statistics, and data interpretation<\/li><li>Working knowledge of publication ethics and guidelines (ICMJE, GPP)<\/li><li>Experience supporting publications for cell therapy, immunology, or rare\/autoimmune diseases<\/li><li>Exceptional scientific writing and editing skills<\/li><li>Strong project management and organizational abilities<\/li><li>Ability to work independently while collaborating effectively across functions<\/li><li>High attention to detail and commitment to quality and compliance<\/li><li>Clear communicator with the ability to manage competing priorities<\/li><\/ul><p><br><\/p><p><\/p>\\n<div>$90 - $110 an hour<\/div>\\n<br\/><br\/>Please mention the word **BLESSING** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-medical-affairs-writer-contract-kyverna-therapeutics-1129320","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-medical-affairs-writer-contract-kyverna-therapeutics-1129320"},{"slug":"remote-executive-director-patient-advocacy-kyverna-therapeutics-1129319","id":"1129319","epoch":1766448165,"date":"2025-12-23T00:02:45+00:00","company":"Kyverna Therapeutics","company_logo":"","position":"Executive Director Patient Advocacy","tags":["director","exec","biotech","healthcare","strategy","non tech"],"description":"<p>Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, <b>Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome<\/b>, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what\u00e2\u0080\u0099s possible.<\/p><p><span style=\"font-size: 11pt;\">&nbsp;<\/span><\/p><p><span style=\"font-size: 11pt;\">Kyverna is seeking an Executive Director, Patient Advocacy, to lead our patient advocacy strategy and outreach efforts. This business-critical role is responsible for building, owning and advancing strategic relationships with patient advocacy organizations across the autoimmune, rare disease and CAR T-cell therapy landscape. The Executive Director will serve as Kyverna\u00e2\u0080\u0099s primary interface with patient communities, to increase disease education and awareness, develop patient support services as needed, promote research and development of new therapies, and drive forward patient-centric public policies.<\/span><\/p><p>&nbsp;<\/p><p><b>Title: <\/b>Executive Director, Patient Advocacy<\/p><p><b>Reports to: <\/b>SVP, Corporate Affairs, Communications and Investor Relations<\/p><p><b>Location: <\/b>Remote Eligible<\/p><p><b>Travel: <\/b>up to 25%<\/p>\\n<p><\/p><p><br><\/p><b>Responsibilities:<\/b><ul><li>Develop and execute a long-term patient advocacy strategy aligned with Kyverna\u00e2\u0080\u0099s corporate objectives and the evolving needs of patient communities.<\/li><li>Serve as a strategic liaison between Patient Advocacy and cross-functional partners including Medical Affairs, Clinical Development, and Commercial to ensure patient insights inform decision-making across the organization, including clinical development strategies and patient support initiatives.&nbsp; <\/li><li>Develop and maintain deep, trusted relationships within the autoimmune and rare disease patient advocacy communities as well as relevant CAR T-cell therapy organizations and associated stakeholders.<\/li><li>Develop and implement programming with patient groups where Kyverna may provide appropriate support and engagement, including, but not limited to, disease awareness campaigns, patient support initiatives, patient roundtables, clinical trial recruitment and public policy work.<\/li><li>Represent Kyverna at key patient advocacy meetings and conferences.<\/li><li>Manage corporate sponsorships, programs and initiatives in partnership with &nbsp;patient advocacy groups. <\/li><li>Develop the relevant patient materials needed to support sponsorships and\/or educational initiatives with patient advocacy groups.<\/li><li>Partner with Corporate Communications and other relevant functions to highlight patient sponsorships and related initiatives internally and externally, as appropriate. &nbsp;<\/li><li>Manage corporate grants to ensure compliance with policies and reporting requirements.<\/li><li>Monitor trends within the patient advocacy community and provide relevant strategic insights and updates to leadership as well as feedback to leadership regarding the patient advocacy community\u00e2\u0080\u0099s perception of the company and associated activities.<\/li><li>Prepare senior leaders for meetings with the patient advocacy community and provide feedback post engagements.<\/li><li>Support Kyverna\u00e2\u0080\u0099s community engagement efforts with charitable organizations.<\/li><li>Ensure compliance with all relevant rules and regulations associated with engagement with non-profit organizations and fulfill any reporting requirements.<\/li><\/ul><p><br><\/p><b>Qualifications<\/b><ul><li>Bachelor\u00e2\u0080\u0099s or Master\u00e2\u0080\u0099s degree in Communications, Business, Life Sciences, Biotechnology, or a related field.<\/li><li>15+ years of experience building and leading patient advocacy relationships and programs with experience in CAR-T, cell therapy, autoimmune, and\/or rare diseases strongly preferred.<\/li><li>Strong track record for partnering and collaborating with business leaders to understand business goals.<\/li><li>Excellent communication skills, with the ability to translate complex scientific data into patient-friendly language.<\/li><li>Ability to build strong relationships and work effectively and credibly with senior leadership and a wide variety of teams across a company.&nbsp; <\/li><li>Strong personal network of patient advocacy relationships.<\/li><li>Understanding of regulations associated with biotech\/pharma companies\u00e2\u0080\u0099 engagement with non-profits and patient advocacy organizations.<\/li><li>Comfortable operating and driving results in a dynamic and highly innovative environment.<\/li><li>Detail-oriented, well-organized self-starter; experienced in managing multiple projects simultaneously; flexibility and results-oriented focus are essential.<\/li><\/ul><p><br><\/p><p><\/p>\\n<p>The base salary range for this position is&nbsp;$275K-$300K annually.&nbsp;This salary range is an estimate of what we reasonably expect to pay for this posted position, and the actual salary may vary based on various factors that may include but are not limited to quality and length of experience, education, geographic location and alignment with market data.&nbsp;<\/p><p>&nbsp;<\/p><p><br><\/p><br\/><br\/>Please mention the word **STABILIZE** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-executive-director-patient-advocacy-kyverna-therapeutics-1129319","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-executive-director-patient-advocacy-kyverna-therapeutics-1129319"},{"slug":"remote-director-medical-information-kyverna-therapeutics-1129316","id":"1129316","epoch":1766448127,"date":"2025-12-23T00:02:07+00:00","company":"Kyverna Therapeutics","company_logo":"","position":"Director Medical Information","tags":["director","medical","biotech","healthcare","senior","strategy","operations","non tech"],"description":"<p>Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, <b>Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome<\/b>, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what\u00e2\u0080\u0099s possible.<\/p><p><br><\/p><p>The Director of Medical Information provides strategic leadership and operational oversight of the Medical Information function across development and commercialization. This role is responsible for ensuring the timely, accurate, balanced, and compliant dissemination of medical and scientific information to external stakeholders, including healthcare professionals, payers, and academic partners, as well as to internal cross-functional teams.<\/p><p><br><\/p><p>The Director will establish, scale, and continuously improve Medical Information capabilities to support pipeline assets and commercial products, while ensuring full alignment with regulatory, legal, and compliance requirements. As a senior scientific leader within Medical Affairs, this individual will serve as a key cross-functional partner and escalation point for complex scientific inquiries.<\/p><p><br><\/p><p> Department: Medical Affairs<\/p><p> Reports To: Scientific Director, Medical Affairs<\/p><p> Location: Remote eligible<\/p><p> Travel: Approximately 10 percent<\/p>\\n<p><\/p><p><br><\/p><b>Responsibilities<\/b><ul><li><span>Defines and executes the global Medical Information strategy aligned with Medical Affairs and company objectives. This includes ownership of scientifically accurate, balanced, current, and compliant medical response content such as standard response documents, FAQs, scientific letters, and medical information platforms.<\/span><\/li><li>Oversees intake, triage, and response to unsolicited medical inquiries, ensuring consistent, high-quality responses within defined service-level agreements. The Director serves as the escalation point for complex or high-impact inquiries and ensures appropriate documentation and governance.<\/li><li>Leads Medical Information readiness for pre-launch and launch activities, including infrastructure development, staffing or vendor resourcing, content creation, training, and system readiness. <\/li><li>Builds and manages a high-performing Medical Information Call Center. This includes vendor oversight, quality assurance, budget management, and performance metrics and KPIs. <\/li><li>Supports scientific exchange at medical congresses, responding to health care provider inquiries at company-sponsored booths<\/li><li>Provides Medical review of company materials in MLR review to ensure scientific accuracy, evidentiary support, and alignment with approved labeling.<\/li><li>Collaborates cross-functionally with Clinical Development, Regulatory Affairs, Pharmacovigilance\/Safety, Legal, Compliance, Commercial, Market Access, and Manufacturing to enable appropriate scientific exchange and maintain separation of promotional and non-promotional activities. <\/li><li>Strategically supports Field Medical teams, including MSL training and content development.<\/li><li>Incorporates emerging clinical data, publications, congress insights, and real-world evidence into Medical Information content, with focus on complex and specialty therapies such as cell and gene therapies. <\/li><li>Ensures inspection readiness and supports audits, responses, and corrective actions related to Medical Information activities.<\/li><\/ul><p><br><\/p><b>Qualifications<\/b><ul><li>Advanced scientific or medical degree is required, such as PharmD, PhD, MD, or equivalent.<\/li><li>A minimum of 12 years of experience in Medical Information, Medical Affairs, or related scientific roles within the pharmaceutical or biotechnology industry is required, along with demonstrated leadership experience managing teams and\/or outsourced Medical Information operations.<\/li><li>Deep knowledge of Medical Information regulations and compliance standards, including FDA, EMA, and applicable global guidance. Experience supporting pre-commercial and launch-phase organizations, as well as product launches and lifecycle management in regulated environments, is required.<\/li><li>Experience with complex or specialty therapies is strongly preferred, including cell therapy, gene therapy, immunology, neurology, oncology, or rare disease. Prior experience building or scaling a Medical Information function in a growing biotech organization is highly desirable. Global or ex-US experience is a plus.<\/li><li>Excellent scientific communication skills, strong strategic thinking, and operational discipline. The ideal candidate will demonstrate sound judgment, credibility with senior leaders and external stakeholders, and the ability to manage complexity in fast-paced, resource-conscious environments.<\/li><\/ul><p><br><\/p><p><\/p>\\n<p><br><\/p><p> The national salary range for this position is $210,000 to $235,000 USD annually. The final compensation will be based on individual qualifications, experience, skills, internal equity, and market alignment. This position is also eligible for an annual bonus, comprehensive benefits, and participation in the Company\u00e2\u0080\u0099s stock option plan.<\/p><p><br><\/p><p><br><\/p><br\/><br\/>Please mention the word **FAV** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Remote","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-director-medical-information-kyverna-therapeutics-1129316","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-director-medical-information-kyverna-therapeutics-1129316"},{"slug":"remote-career-syngenta-1129244","id":"1129244","epoch":1765900819,"date":"2025-12-16T16:00:19+00:00","company":"Syngenta","company_logo":"","position":"Career","tags":["biotech","non tech","other"],"description":"Find your next job Syngenta, you\u00e2\u0080\u0099ll play a vital role in safeguarding global food security and shaping the future of agriculture.<br\/><br\/>Please mention the word **SUSTAINABLE** and tag ROjox when applying to show you read the job post completely (#ROjox). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.","location":"Not specified","apply_url":"https:\/\/remoteOK.com\/remote-jobs\/remote-career-syngenta-1129244","salary_min":0,"salary_max":0,"logo":"","url":"https:\/\/remoteOK.com\/remote-jobs\/remote-career-syngenta-1129244"}]