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Healthcare
› Medical Writing
Medical Writing
705 open positions
Manager, Professional Education and KOL Engagement
Envista
United States of America, California, Brea
$130k–$130k
1mo
Develops and executes global professional education, KOL engagement, and customer education strategies to drive portfolio growth and product adoption in the medical device industry.
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Senior Scientific Director / Executive Medical Director, Medical Affairs – Hematology
AbbVie
Mettawa, IL, us
1mo
Senior leadership role driving medical and scientific strategy, operational execution, and stakeholder engagement for hematology assets (Epcoritamab and Ibrutinib) within Medical Affairs.
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Associate Director, Medical (Pharma Ad Agency Experience Required)
Eversana
New York, NY, us
1mo
Lead medical strategy and content development for pharma clients by translating complex clinical data and scientific literature into compelling narratives and educational materials for healthcare professionals.
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Senior Analyst Medical Insights
Sanofi
Hyderabad
1mo
Generate actionable medical insights and intelligence to support strategic decision-making across Sanofi's medical affairs, commercial, and brand teams.
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Regulatory Affairs Manager CMC
Viatris
Northern Cross, Dublin, Ireland
1mo
Independently prepare regulatory assessments and contribute to global regulatory strategies for the Upjohn product portfolio across the drug development and manufacturing lifecycle.
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Medical Manager
Pg
MUMBAI GENERAL OFFICE
1mo
Design and deliver medical affairs activities for the assigned therapeutic area, ensuring scientific excellence and compliance while engaging healthcare professionals and organizations.
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Medical Manager
Sanofi
Shanghai
1mo
Develop and execute medical strategies and plans to provide scientific support for new and existing pharmaceutical products, focusing on unmet medical needs and value proposition.
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Manager-Alliance
Amgen
Japan - Tokyo
1mo
Manage strategic alliances and partnerships with external organizations to maximize contract values and ensure governance compliance.
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Associate Director, CMC
Msd
CHN - Beijing - Beijing (Wangjing Park), CN
1mo
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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Manager, CMC Regulatory Affairs
Regeneron
Tokyo, JP
1mo
Lead regulatory CMC activities for CTN, J-NDA, and eCTD supplement submissions in Japan, acting as a liaison with the PMDA.
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International CMC Regulatory Affairs Manager I
AstraZeneca
India - Bangalore
1mo
Manage the production of Chemistry, Manufacturing and Control (CMC) documentation and project manage international regulatory submissions for synthetics and biologics.
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Senior Scientific Writer HEVA
Sanofi
Hyderabad
1mo
Create HEVA communications deliverables (manuscripts, posters, abstracts, slide decks) and maintain Core Value Decks to support access and reimbursement decisions.
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Senior Regulatory Scientist
Icon
Remote
1mo
Provide advanced regulatory and scientific expertise to support global clinical development strategies, submissions, and health authority interactions.
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Med Info Spec I - Mid shift & Hybrid
Thermofisher
Taguig City, Philippines
1mo
Providing medical and technical information to healthcare providers and patients regarding pharmaceutical or device products, including answering inquiries on dosage, side effects, and collecting adverse event reports.
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Associate Director, Global Medical Neuroscience, Medical Communications
Bristolmyerssquibb
Princeton - NJ - US
1mo
Develop and execute medical communications strategies for Neuroscience therapeutic areas, ensuring scientifically rigorous and ethically grounded content across drug development and commercialization.
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Medical Writer
Alimentiv
Toronto, Ontario
1mo
Provide medical writing services and consultation to Clinical Research Scientists, Academic partners, Sponsors, and the Corporation by researching, writing, reviewing, and editing scientific information for regulatory documents and presentations.
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Senior Manager, RA TA Group, Regulatory Affairs(Neurology)
AbbVie
Minato City, Tokyo, jp
1mo
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
1mo
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 Specialist, Nonclinical Medical Writing
Msd
USA - California - South San Francisco (Grand Ave)
$131k–$131k
1mo
Generate preclinical reports and regulatory submission modules to support drug development programs from FIH to global marketing applications.
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US Director Medical Affairs (USDMA): Rheumatology/Dermatology (Remote)
Msd
Remote
1mo
US Director of Medical Affairs leading strategy and execution for Rheumatology and Dermatology therapeutic areas, driving scientific exchange, trials, and field readiness.
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Medical Director, Dermatology
Sanofi
Cambridge, MA, US
1mo
Lead the development and execution of the US medical/scientific strategy for Dermatology products, serving as the product expert and strategic partner to Clinical, Commercial, Regulatory, and Market Access teams.
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Senior Medical Director, Medical Affairs, Neurology
Regeneron
SLEEPY HOLLOW, US
$333k–$333k
1mo
Lead medical strategy and execution for Neurology/Myasthenia Gravis, serving as a key scientific resource for product development and patient safety.
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Squad Business Partner
Roche
South San Francisco, US
$161k–$161k
1mo
Design and deliver training programs and continuous education for field-based Customer Engagement teams to ensure consistent execution of squad strategies and product knowledge.
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Manager, Senior Manager, Public Affairs
Novartis
Toranomon (NPKK Head Office)
1mo
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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Associate Director, Publications
Regeneron
SLEEPY HOLLOW, US
$157k–$157k
1mo
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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Senior Manager, Regulatory Affairs US Advertising and Promotion - Immunology - Hybrid
AbbVie
Florham Park, NJ, us
1mo
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–$145k
1mo
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
1mo
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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Senior Manager, Regulatory Affairs
Regeneron
Tokyo, JP
1mo
Lead Japan regulatory strategies and PMDA consultations for oncology and other therapeutic areas, managing marketing applications and post-approval changes.
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Associate Director, Regulatory Labeling and Disclosures
Sarepta
United States
$161k–$161k
1mo
Leading global labeling activities and clinical trial disclosures for development and marketed gene therapy products.
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Associate Manager, CMC Regulatory Affairs
Regeneron
Tokyo
1mo
Support regulatory CMC strategy and submissions for the Japan organization, including planning, scientific writing, and critical review of CTN, J-NDA, and eCTD supplements.
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Marketing Operations Manager
Vrtx
Boston, MA
$120k–$120k
1mo
Lead and subject matter expert for Communications Review Committee (CRC) teams, managing the review, approval, production, and distribution of branded and non-branded communications in a regulated environment.
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Senior Director, Regulatory Clinical Strategy
Pacira BioSciences
Parsippany, New Jersey
$203k–$203k
1mo
Directs and implements global regulatory projects and clinical strategy for non-opioid pain management and regenerative health solutions.
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Associate Director, RA-CMC PAC DM
AbbVie
North Chicago, IL, us
1mo
Manage and author Chemistry, Manufacturing, and Control (CMC) sections for marketed product variations and post-approval change submissions to ensure regulatory file-ability and acceptance.
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VP, Medical Strategy
Klick
Philadelphia, Pennsylvania, us
1mo
Strategic scientific partner for pharma/life sciences clients shaping brand strategy, medical communications, and commercialization initiatives.
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Medical Content Development Manager / Team Lead
Eversana
Milan, Lombardy, it
1mo
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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Medical Advisor-Inhale
AstraZeneca
China
1mo
Provide medical input for life cycle management of priority brands and therapeutic areas to address unmet medical needs.
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Director, Global Scientific Communications, Hematology
AstraZeneca
US - Boston - MA
$231k–$231k
1mo
Lead global scientific communications strategy, publication planning, and medical education for a high-impact Hematology portfolio in rare diseases.
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Executive Director, Global Medical Affairs
Eversana
Overland Park, KS, us
1mo
Senior leader shaping and executing Global Medical Affairs strategy, operations, and thought leadership for biopharmaceutical clients across oncology, hematology, rare disease, immunology, neurology, and cardiology.
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Proposal Writer I
Eversana
Yardley, PA, us
1mo
Lead and contribute to the development of proposals, RFIs, and related documents for pharmaceutical clients, collaborating with cross-functional teams to align sales strategy and deliver client-ready content.
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Medical Copywriter
Inizioevoke
Inizio Evoke - London
1mo
Transform complex clinical and scientific data into compliant, persuasive promotional copy for healthcare professionals, payers, and direct-to-patient audiences across digital, print, video, and interactive formats.
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Senior Manager, Regulatory Affairs
AbbVie
Maidenhead, ENGLAND, gb
1mo
Senior Manager leading the UK Regulatory Affairs team for a specific therapeutic area, ensuring MHRA compliance and driving product lifecycle strategies.
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Regulatory Affairs Manager Advertising and Promotion
AbbVie
Marlow, England, gb
1mo
Provides international regulatory expertise, perspective, and leadership for pharmaceutical advertising and promotion, ensuring compliance with global codes and regulations while balancing business needs with risk.
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VP, Medical Science & Strategy - Rare Disease
Thermofisher
Remote, North Carolina, USA
1mo
Define and govern rare disease portfolio strategy, translating market needs into growth priorities and investment choices for Thermo Fisher Scientific's clinical research business.
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EU Senior Global Reg Affairs Project Leader (m/f/d)
Viatris
Allschwil-Office
1mo
Define and execute EU regulatory strategies, lead submissions, and serve as primary contact with EMA and National Competent Authorities for a global healthcare company.
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Sr. Manager, Regulatory Affairs
Alnylam
Japan
1mo
Senior Manager leading regulatory strategy, submissions, and lifecycle management for development and commercial programs in Japan.
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Manager, Promotional Review Committee (PRC)
Gilead
United States - California - Foster City
$136k–$136k
1mo
Lead end-to-end promotional review operations for assigned brands, managing the lifecycle of marketing materials in Veeva Vault PromoMats and facilitating review committees.
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Director, Medical Training
AstraZeneca
US - Wilmington - DE
1mo
Define and execute enterprise-wide clinical learning strategy for Medical teams to build scientific and clinical capabilities for patient impact and healthcare systems.
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Editor
Inizioevoke
Remote
$58k–$58k
1mo
Copyediting, fact-checking, and proofreading promotional, digital, and medical communications materials for pharmaceutical and life science clients.
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Director, Head of Global Nemluvio Regulatory Strategy
Galderma
Boston
$200k–$200k
1mo
Leads global regulatory strategy, submission planning, and health authority engagement for Nemolizumab (Nemluvio) across approved and development-stage indications.
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