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Healthcare
› Medical Writing
Medical Writing
733 open positions
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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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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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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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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Medical review and affairs manager
Sobi
Zug, ZG, ch
1mo
Act as the legally required Person Responsible for Advertising in Switzerland, ensuring promotional and non-promotional materials are scientifically accurate, balanced, and compliant with Swiss regulations.
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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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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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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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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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Medical Lead CEE+
Sobi
Ljubljana, Ljubljana, si
1mo
Lead regional medical affairs planning and execution, KOL engagement, and scientific data generation for assigned medicinal products in the CEE+ region.
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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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Senior Medical Affairs Manager
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Abbott
40, TH
1mo
Senior Medical Affairs Manager providing medical/scientific expert advice, developing education programs, and managing clinical research activities for assigned therapeutic areas.
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Head, US PA&PA Immunology
↗
Sanofi
Cambridge, MA, US
1mo
Lead US Public Affairs & Patient Advocacy strategy for Sanofi's Immunology portfolio, focusing on Dupixent and pipeline assets to accelerate patient access and outcomes.
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Global Medical Head - Integrated & Strategic Evidence Generation
↗
Ucb
Slough, ENG, GB
1mo
Drive the development and execution of integrated evidence generation plans for designated medicines and indications to create patient value.
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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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Medical Manager - CNS
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Azurity Pharmaceuticals - Us
Woburn, MA, US
1mo
Lead and execute medical strategy to support the safe, effective, and evidence-based use of CNS products, serving as a scientific expert and liaison between internal teams and external stakeholders including HCPs and KOLs.
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Medical Director- Rheumatology, Sponsor Dedicated
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Iqvia
Remote
1mo
Provide medical, clinical, and scientific advisory expertise to IQVIA divisions, serving as a medical expert during the project delivery lifecycle.
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Director, Global Medical Cardiovascular, Medical Product Lead
Bristolmyerssquibb
Princeton - NJ - US
1mo
Strategic leader responsible for developing and executing global medical affairs strategy for a next-generation cardiac myosin inhibitor in heart failure and cardiomyopathy.
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Regulatory Affairs Supervisor
AbbVie
Taipei, tw
1mo
Manage registration of new products and variations to obtain and maintain marketing approvals for AbbVie products in Taiwan, ensuring compliance with local regulations and supporting clinical research and product launches.
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Medical Affairs Manager COPD
Gsk
Belgium-Wavre
$91k–$91k
1mo
Drive medical strategy and execution for the COPD portfolio in BeLux, focusing on specialty assets and providing scientific insight to stakeholders.
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Medical Engagement Manager Launches
Sanofi
Warsaw
1mo
Develop and implement local medical strategies for novel drugs in Autoimmune Diabetes, establishing credibility with the scientific community and shaping long-term treatment paradigms.
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Director, Medical Information
Xenon
Boston
1mo
Establish, scale, and evolve the Medical Information function to manage medical inquiries, develop scientific response content, and operate contact center/digital capabilities for healthcare professionals and patients.
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Senior Medical Writer/Principal - Regulatory Documents
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サイネオス・ヘルス
Remote
1mo
Lead the clear and accurate completion of complex regulatory medical writing deliverables for drug development and commercialization, ensuring scientific information is presented clearly and accurately.
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Client dedicated Global Regulatory Lead
Thermofisher
Remote, Belgium
1mo
Global Regulatory Lead serving as a business partner and facilitator for regulatory activities across the product lifecycle, from pre-approval to post-approval commercialization.
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Director, Regulatory Affairs (Regulatory Strategy)
Icon
Canada, Burlington
1mo
Develop and implement regulatory strategies for drugs, biologics, and combination products for current and prospective clients in Canada.
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Account Supervisor, CME
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Ogilvy
Barcelona, CT, ES
$65k–$65k
1mo
Oversee project delivery and supervise teams to ensure high-quality medical education programs and materials are delivered on time and on budget for healthcare clients.
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Medical Affairs Consultant
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Syneos Health Commercial Solutions
Buenos Aires, Buenos Aires Province, Argentina
1mo
Provide medical affairs strategy insights to pharmaceutical and biotech customers by summarizing complex scientific ideas and data into influential storyboards for business leaders.
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Medical Director (Publications)
↗
Real Chemistry
Remote
$130k–$150k
1mo
Lead scientific strategy and content delivery for publication and broader medical affairs deliverables, serving as a senior scientific partner to clients in pharma/biotech.
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Medical Manager Onco- Hematología
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Pfizer
Bogotá, CUN, CO
1mo
Provides medical and scientific support to internal teams and external stakeholders including investigators and regulatory authorities for oncology products.
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Consulting Associate/Strategy & Medical Affairs (Life Sciences)
Charlesriverassociates
Toronto, Canada
$120k–$140k
1mo
Deliver consulting, strategic marketing, and medical affairs support to life sciences clients including pharmaceutical and biotechnology companies.
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Director, Medical Writing
Dynetherapeutics
Remote
$190k–$190k
1mo
Strategic leadership and hands-on execution for developing high-quality, compliant clinical and regulatory documents supporting drug development programs for neuromuscular diseases.
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Medical Affairs, Medical Advisor (Influenza)
Msd
JPN - Tokyo - Chiyoda, JP
1mo
Creating and executing Country Medical Affairs Plans (CMAP) for Influenza products, managing scientific insights, and leading medical education programs.
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Internal Medical Translator (English > Korean)
↗
Iqvia
São Paulo, SP, BR
1mo
Linguistically and culturally interpret written life sciences materials, maintaining original structure and style while ensuring accuracy of ideas and facts.
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Director Medical Innovation & Liaison Pharma (m/f/d)
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Fresenius Kabi
Bad Homburg vor der Höhe, HE, DE
1mo
Strategic Medical Affairs leadership combining innovation scouting, business development support, and portfolio strategy for global injectable and IV products.
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Global Medical Affairs, Medical Director- Chronic Weight Management
↗
Amgen
Remote
$221k–$299k
1mo
Lead global medical affairs strategy for Chronic Weight Management assets, driving evidence generation, medical communication, and external engagement across the product lifecycle.
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Manager, Regulatory Affairs
↗
Alexion Pharmaceuticals
Mississauga, ON, CA
$107k–$141k
1mo
Lead regulatory strategies and submissions for assigned drug and biologic product portfolios to Health Canada.
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Principal Medical Writer
Realchemistry
London
1mo
Co-lead the creation of high-quality medical content and provide strategic insights to elevate client deliverables across various therapy areas in the pharmaceutical and biotech industries.
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Sr. RA Specialist
AbbVie
Seoul, Seoul, kr
1mo
Manage preparation of regulatory submissions to obtain approvals and provide regulatory input on matters for company products.
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