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Healthcare
› Medical Writing
Medical Writing
1,297 open positions
Medical Writing Manager (Hybrid)
Vrtx
Boston, MA
$120k–$180k
2mo
Lead Medical Writing Scientist preparing moderately complex clinical and regulatory documents for clinical studies.
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Medical Director (m/w/x)
Doctorflix
Berlin
2mo
Lead the medical content catalog and format development for one of Germany's largest CME learning platforms, ensuring evidence-based medical knowledge reaches thousands of physicians.
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Medical Writer Assitant (Trainee)
Omnicomhealth
Remedy Edge - Barcelona
2mo
Support medical strategy and scientific content creation for healthcare clients.
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Senior Medical Writer
Omnicomhealth
Remedy Edge - Barcelona
2mo
Develop scientifically rigorous and creatively engaging communication materials supporting clients' medical and promotional strategies.
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Regulatory Affairs Associate Director - EU Regulatory Lead - FSP Client Dedicated
Thermofisher
Remote, Belgium
2mo
Lead EU regulatory strategy and execution for a dedicated pharmaceutical client, guiding product development from preclinical stages through registration and commercialization across Europe and select territories.
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顧問類-專員/資深專員(生技產業)
PwC
Taipei, TW
2mo
Research and write reports/articles on biotech/medical trends; plan and execute professional lectures and international forums; maintain relationships with industry KOLs.
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Senior Labeling Hub Manager
Viatris
Lisbon, Lisbon, Portugal
2mo
Develop and execute labeling strategies and project plans for generic and branded pharmaceutical products across the European Economic Area, ensuring compliance with regional regulations and supporting end-to-end artwork implementation.
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US Senior Medical Director, Autoimmune T1D
Sanofi
Morristown, NJ
2mo
Develop and execute US medical strategy for autoimmune Type 1 Diabetes products, including scientific field communications, publications, advisory boards, and data generation.
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Senior Manager RA US Advertising and Promotion - Hybrid
AbbVie
North Chicago, IL, us
2mo
Senior Manager leading Regulatory Affairs for US Advertising and Promotion in Neuroscience, ensuring compliance with FDA and industry guidelines while influencing regulatory policy.
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Senior Manager RA US Advertising and Promotion - Hybrid
AbbVie
Irvine, CA, us
2mo
Senior Manager leading Regulatory Affairs for US Advertising and Promotion in Neuroscience, ensuring compliance with FDA and industry guidelines while influencing regulatory policy.
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Director Regulatory Affairs ANZ
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Csl
Melbourne, Victoria, Australia
2mo
Lead national regulatory operations and strategy for CSL's biotechnology products in Australia and New Zealand, serving as the primary interface with Health Authorities and industry bodies.
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Director, Publications
Regeneron
SLEEPY HOLLOW, US
$183k–$305k
2mo
Lead strategic direction and operational performance of publication plans for therapeutic assets, collaborating with authors, medical affairs partners, and external agencies.
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Partnership Manager Australia (Medical Doctor)
Amboss
Remote
2mo
Represent AMBOSS at events and conferences across Australia to introduce and grow the platform among medical students and early-career doctors.
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Associated Director International Learning Immunology Gastro Portfolio
AbbVie
Mettawa, IL, us
2mo
Strategic partner to Gastro portfolio Brand teams to assess learning needs, develop learning strategies, and ensure portfolio strategy is represented in all learning programs and solutions.
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Senior Director, Medical Affairs Learning & Development
Dynetherapeutics
Waltham, MA
2mo
Define and execute Medical Affairs learning and capability-building strategy to equip teams for commercialization, launch readiness, and compliant engagement with healthcare professionals.
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Head, Regulatory Affairs, General Medicine and Vaccines Canada
Sanofi
Toronto, ON
2mo
Provide leadership to a team of regulatory professionals for regulatory affairs activities including early approvals and regulatory compliance throughout the product lifecycle for General Medicine and Vaccines portfolios.
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Freelance- Translators/Linguists, Swedish into English
Iqvia
Remote
2mo
Freelance translator converting Swedish life sciences content into English, including clinical trial documents.
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Job Posting Title Freelance- Translators/Linguists, Cebuano into English
Iqvia
Remote
2mo
Freelance translation of life sciences content, specifically clinical trial documents, from Cebuano to English.
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Scientific Services Lead - Medical Communications
Pobl
Remote
2mo
Lead scientific services and medical communications for local and international projects in publications, medical affairs, and medical education.
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EP & Transplant Medical Head
Sanofi
Tokyo
2mo
Provide senior strategic leadership for kidney transplantation and established portfolio within General Medicines, driving cross-functional excellence to deliver patient outcomes.
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Senior Medical Director
Publicis Groupe Holdings B.V
Philadelphia, Pennsylvania; New York, New York
$107k
2mo
Oversees accuracy and relevance of content for pharmaceutical, biotechnology, and device clients; develops healthcare professional marketing strategies and tactics.
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Senior Medical Director
Publicis Groupe Holdings B.V
Philadelphia, Pennsylvania; New York, New York
$107k
2mo
Oversees accuracy and relevance of content for pharma/biotech/device clients and develops healthcare professional marketing strategies.
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Account Manager, Scientific Visualization and Experiential Engagement (RadScience)
Realchemistry
Remote
$70k
2mo
Account Manager supporting the RadScience team in healthcare communications, managing project operations, client relationships, and new business proposals for scientific visualization and experiential engagement.
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Regulatory Affairs Manager – Ad/Promo SME & Product Specialist
Iqvia
Bucuresti, Romania
2mo
Subject matter expert for advertising and promotion, promotional material review, labelling, and artwork activities within the pharmaceutical and biotechnology industry.
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Manager, Regulatory Affairs Project Management
Bms
Indianapolis - RayzeBio - IN
$135k–$163k
2mo
Plan, execute, and drive regulatory submissions (INDs, NDAs, CTAs) and manage cross-functional timelines for oncology radiopharmaceutical therapies.
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Associate Director, Regulatory CMC
Praxisprecisionmedicines
Remote
$175k
2mo
Planning, preparation, and execution of Chemistry, Manufacturing, and Controls (CMC) regulatory activities for investigational and commercial small molecule and antisense oligonucleotide (ASO) products.
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Manager-Alliance
Amgen
Japan - Tokyo
2mo
Manage strategic alliances with external partners to maximize contract values, ensure governance compliance, and drive growth initiatives for Amgen's pharmaceutical products.
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Medical Governance Manager 80% - 100 %
AstraZeneca
Switzerland - Baar
2mo
Ensure promotional and non-promotional activities, scientific communications, events, and stakeholder interactions comply with internal policies, industry codes, and applicable regulations.
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Medical Writer
Realchemistry
Edinburgh
2mo
Create outstanding medical content across various therapy areas for pharmaceutical and biotech clients, adapting writing styles for different audiences and ensuring compliance with industry guidelines.
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Med Info Spec I - Mid shift & Hybrid
Thermofisher
Taguig City, Philippines
2mo
Provide medical and technical information to healthcare providers and patients regarding pharmaceutical or device products, and manage adverse event reports and product complaints.
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Manager, CMC Regulatory Affairs
Regeneron
Tokyo, JP
2mo
Lead regulatory CMC activities for CTN, J-NDA, and eCTD submissions in Japan, acting as a liaison with the PMDA.
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Associate Director, CMC
Msd
CHN - Beijing - Beijing (Wangjing Park), CN
2mo
Lead the China RA CMC team to deliver timely regulatory submissions and ensure compliance with external regulations and internal quality procedures.
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Senior Manager, RA TA Group, Regulatory Affairs(Neurology)
AbbVie
Minato City, Tokyo, jp
2mo
Leading a Regulatory Affairs Therapeutic Area team in Japan to ensure effective workflow, optimal productivity, and delivery of high-quality regulatory outputs for neuroscience products.
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GRA Labelling Specialist
Sanofi
Hyderabad
2mo
Prepare and coordinate regulatory labeling documents (CCDS, USPI, EU SmPC) for marketed pharmaceutical products, ensuring compliance with health authority regulations and supporting global regulatory strategy.
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Senior Medical Director, Medical Affairs, Neurology
Regeneron
SLEEPY HOLLOW, US
$333k–$451k
2mo
Co-develop medical strategy and execute medical affairs activities for Neurology/Myasthenia Gravis medicines, serving as a key scientific resource for internal teams and external stakeholders.
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Associate Director, Publications
Regeneron
SLEEPY HOLLOW, US
$157k–$257k
2mo
Lead the development and execution of aligned dissemination plans for clinical, HEOR/RWE, PKPD, and disease state publications to ensure research reaches the community accurately and on time.
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Squad Business Partner
Roche
South San Francisco, US
$161k–$300k
2mo
Develop, deliver, and manage training and continuous education for field-based Customer Engagement teams on dedicated squad strategies, ensuring consistent messaging and skill development.
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Manager, Senior Manager, Public Affairs
Novartis
Toranomon (NPKK Head Office)
2mo
Lead Public Policy Engagement (PPE) activities in Japan to maximize product value, shape the external policy environment, and support broader Public Affairs priorities.
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Senior Manager, Regulatory Affairs US Advertising and Promotion - Immunology - Hybrid
AbbVie
Florham Park, NJ, us
2mo
Senior Manager leading Regulatory Affairs for US Advertising and Promotion in Immunology, ensuring compliance with FDA and industry guidelines while influencing regulatory policy.
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Senior Manager, Regulatory Operations
Parabilismed
Cambridge
$145k
2mo
Lead global regulatory submissions, regulatory information management, and publishing operations for a clinical-stage biopharmaceutical company developing alpha-helical peptide medicines.
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Associate Director, International ICEX Content Excellence Strategy Lead
AbbVie
Mettawa, IL, us
2mo
Oversees the International Content Excellence framework across multiple Therapeutic Areas and Affiliates to manage, optimize, and align content processes with Brand Strategy and compliance.
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Associate Manager, CMC Regulatory Affairs
Regeneron
Tokyo
2mo
Support regulatory CMC strategy and submissions for the Japan organization, including CTN, J-NDA, and eCTD supplements.
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Associate Director, Regulatory Labeling and Disclosures
Sarepta
United States
$161k–$201k
2mo
Leading global labeling activities and clinical trial disclosures for development and marketed products in the genetic medicine sector.
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Senior Manager, Regulatory Affairs
Regeneron
Tokyo, JP
2mo
Lead Japan regulatory strategies and PMDA consultations for oncology and other therapeutic areas, managing marketing applications and post-approval changes.
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Senior Director, Regulatory Clinical Strategy
Pacira BioSciences
Parsippany, New Jersey
$203k
2mo
Directs and implements global regulatory projects and clinical strategy for non-opioid pain management and regenerative health solutions.
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Senior Manager, CMC Regulatory (CMC Senior Expert, CMC Regulatory)
Bms
Otemachi-JP
2mo
Senior Manager leading CMC regulatory strategy, risk assessment, and submission execution (CTN, JNDA/sJNDA, CTD) for pharmaceutical development in Japan, bridging global teams and local authorities.
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STAGE Affaires Réglementaires Pharmaceuticals (H/F/NB)
Bayer
Lyon,Rhône,France
2mo
Intern role supporting the Regulatory Affairs team in ensuring the development, registration, and availability of pharmaceutical products for patients in compliance with regulatory requirements.
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Medical Omnichannel Content Manager Oncology - CDI - H/F
Pierrefabre
Hauts-de-Seine (92)
2mo
Translate medical strategies into omnichannel journeys for healthcare professionals (physicians and pharmacists) and produce/manage HCP journey content end-to-end.
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Medical Content Development Manager / Team Lead
Eversana
Milan, Lombardy, it
2mo
Lead medical content development engagements for pharmaceutical and medical device clients, creating scientifically rigorous response documents, FAQs, slide sets, and training materials.
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PR & Media Relations Expert (m/f/d)
Rentschler Biopharma SE
Laupheim, BADEN_WUERTTEMBERG
2mo
Manage external visibility and reputation for Rentschler Biopharma in biopharmaceutical media and stakeholder environments.
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