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Healthcare
› Medical Writing
Medical Writing
1,297 open positions
Medical Writer, Market Access
Precisionmedicinegroup
Remote
$65k–$85k
15d
Develop medically accurate content (flashcards, leave-behinds, training resources) for pharmaceutical clients and managed care audiences.
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Copy Supervisor
Klick
Philadelphia, Pennsylvania, us
15d
Guide creative development of concepts and copy across channels for healthcare brands, ensuring messaging accuracy and clinical clarity.
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Medical Writing Intern, Medical Communications
Precisionaq
Remote
15d
Paid 100% remote internship for upcoming PhD/PharmD graduates to learn medical writing principles and create content for diverse audiences including healthcare professionals and patients.
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Medical Writing Intern, Medical Communications
Precisionmedicinegroup
Remote
15d
Paid 100% remote internship for upcoming PhD/PharmD graduates to learn medical writing principles and create content for diverse audiences (healthcare professionals, patients) in the pharmaceutical industry.
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Expert Pharma Academy & Pharmaceutical Standards (m/w/d)
Redcare-Pharmacy
Sevenum, nl
15d
Managing a digital knowledge database for pharmaceutical standards and optimizing structured onboarding processes for new employees.
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Medical Editor
BGBx
Ontario, Canada
CA$70k–CA$83k
15d
Ensures editorial integrity and factual accuracy of marketing materials for pharmaceutical and life science clients, ensuring compliance with AMA style and FDA regulations.
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Medical Science Liaison T06
AbbVie
Xi'An, Shaanxi, cn
15d
Maintain updated medical knowledge, create and deliver medical training materials, coordinate PPD medical projects, and provide medical advice on product communication.
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Medical Affairs Manager
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Artech
New Delhi, Delhi, India
15d
Lead Medical Affairs initiatives for medical devices or pharmaceutical products, leveraging expertise in hematology, apheresis, or cell therapy.
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Regulatory Manager (CMC and Biologics)
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Syneos Health
TS, IN
15d
Manage regulatory submissions and project teams for biologics, biosimilars, and CMC across global markets, authoring dossiers and advising clients on compliance.
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Senior Project Manager - Medical Affairs
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Revcats
Remote
15d
Lead end-to-end Medical Affairs initiatives, turning medical strategy into coordinated, compliant action for pharmaceutical/biotech organizations.
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Health Economics Consultant
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Parexel
Remote
15d
Conduct and analyze research to develop strategic recommendations and systematic literature reviews for clients in the healthcare and pharmaceutical industry.
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PPSM Sr Analyst
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Accenture
TN, IN
15d
Develop competitive, technically accurate, and commercially compelling proposals for R&D services in the Life Sciences sector, combining expertise in Clinical, Pharmacovigilance, and Regulatory domains.
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Evidence Generation Lead (Medical Affairs) / PH / São Paulo/SP
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Bayer
São Paulo, SP, BR
15d
Lead the implementation of local evidence generation strategy and projects (Phase IV, non-interventional, RWE) to support Bayer's pharmaceutical portfolio and patient outcomes.
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Associate Director, Global Policy Strategy Execution
Bms
Princeton - NJ - US
$182k–$221k
15d
Shape and execute BMS' global policy agenda by developing strategies, evidence-based positions, advocacy tools, and thought leadership content to support business priorities and strengthen credibility with external stakeholders.
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International Medical Education Trainee
Alcon
Barcelona, Spain
15d
Coordinate and execute international medical education initiatives for healthcare professionals, including KOL development and congress strategy.
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Medical Affairs Manager, South East Asia
Galderma
Petaling Jaya, MY
15d
Provide medical oversight for all medical affairs activities across Galderma's South East Asia cluster (Malaysia, Singapore, Indonesia, Vietnam) for Prescription, Aesthetics, and Consumer business units.
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Life Sciences Consultant
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Alten
Lisbon, Portugal
15d
Consultant supporting Life Sciences clients in pharmaceutical, medical device, and cosmetics sectors.
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U.S. Medical Director - Immunology
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Sanofi
Cambridge, MA
15d
Lead U.S. medical strategy, evidence generation, and external stakeholder engagement for immunology therapeutic products.
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U.S. Medical Director - Immunology
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Sanofi
Morristown, NJ
15d
U.S. Medical Director leading medical strategy, evidence generation, and external stakeholder engagement for immunology therapeutic products.
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Life Science specialist
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PatSnap
Singapore, Singapore
15d
Monitor pharmaceutical pipelines and regulatory developments across China, Japan, US, Europe, and Australia; verify AI-generated research and maintain structured records of drug programs.
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Medical Operations & Engagement Manager
Sanofi
Seoul, KR
15d
Manage medical operations and engagement for vaccine franchises in South Korea, overseeing Post-Marketing Surveillance (PMS) programs, field medical excellence frameworks, and external stakeholder engagement.
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Senior Specialist Regulatory Affairs (Oncology)
Msd
MEX - Federal District - Mexico City
15d
Ensure timely preparation and submission of new Marketing Authorization applications and maintain regulatory status for oncology products with Mexican Health Authority (COFEPRIS).
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Head of Diagnostics
AstraZeneca
Turkey - Istanbul, TR
15d
Lead diagnostics strategy and Medical Affairs activities to strengthen diagnostics' role in the patient journey for complex diseases.
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Regulatory Affairs Mgr
Amgen
Japan - Tokyo
15d
Develop and execute regulatory strategies to obtain and maintain clinical trial and marketing licenses for Amgen molecules in Japan, interfacing with local authorities (MHLW/PMDA) and aligning with global strategy.
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Stagiaire / Alternant(e) Affaires Médicales
Biibhr
Paris, France
15d
Support the creation and execution of Medical Affairs events (symposiums, digital and non-digital PR), coordinate with product core teams, and develop training content for sales teams.
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Senior Director, Regulatory Affairs, CMC
Xenon
Boston
15d
Provide strategic regulatory CMC leadership for major development or commercial assets, serving as a senior advisor to cross-functional teams on global regulatory submissions and agency interactions.
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Area Medical Director, EEMEAP (m/f/d)
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Abbott
Wiesbaden, HE, DE
15d
Provide strategic medical leadership for Medical Affairs across the EEMEAP region (Eastern Europe, Middle East, Africa, and Pakistan), translating clinical evidence into actionable priorities and serving as the senior medical authority for internal and…
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Associate Program Director, Commercial Regulatory Affairs (CORA)
Roche
South San Francisco, US
$120k
15d
Lead Commercial Regulatory Affairs (CORA) committees and provide regulatory support for assigned products, cross-portfolio activities, and promotional material development within the global Pharma Division.
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Medical Director - OBU, Rare Diseases and Diagnostics
AstraZeneca
, Bangkok, Thailand
15d
Strategic leadership of the Medical Affairs function in Thailand for OBU, Rare Diseases, and Diagnostics, focusing on business planning, team management, and scientific partnerships.
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Head of Diagnostics
AstraZeneca
Şişli, İstanbul, Türkiye
15d
Lead diagnostics strategy and Medical Affairs activities to strengthen the role of diagnostics within the patient journey.
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SPECIALIST PROGRAM MANAGER LATAM
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Abbott
Cali, VAC, CO
15d
Lead end-to-end management of strategic pharmaceutical development programs across Latin America, from Business Case definition to commercial launch.
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Associate Director, Global Policy Strategy Execution
Bristolmyerssquibb
Princeton - NJ - US
$182k–$221k
15d
Shape and execute Bristol Myers Squibb's global policy agenda by developing strategies, evidence-based positions, and advocacy tools to support business priorities and strengthen credibility with external stakeholders.
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Senior Program Manager - Medical Content - Ostro
Veeva
Remote
$100k–$150k
16d
Own end-to-end quality of medical content deliverables for AI-powered patient/HCP engagement tools, managing contractor editors and guiding content through regulatory review.
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Medical Writer – Scientific and Regulatory Documents
MNC JOBS INFO
Singapore
16d
Translate complex medical, clinical, and scientific information into clear, accurate, and well-structured documents for healthcare professionals, researchers, and regulatory authorities.
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Labeling Operations Manager, Associate Consultant
ClinChoice
Colombia- Bogota
16d
Provide operational support for the creation and updates of regulatory labeling documents (CDS, USPI, SPC) and patient labeling for pharmaceutical products.
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Senior Associate, Product Information/Claims Support
ClinChoice
United States
16d
Senior Associate responsible for product information management, claims support, and regulatory dossier preparation in the pharmaceutical industry.
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Senior Scietist or Scientific Advisor or Medical Advisor, aPD
AbbVie
Minato City, Tokyo, jp
16d
Senior medical/scientific advisor responsible for developing medical strategy, driving evidence generation, and providing scientific expertise for assigned products and therapeutic areas.
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Sr. Principal Medical Affairs, BDI Surgery CASAJ
Becton Dickinson Medical Devices
Singapore
16d
Develop strategic partnerships with scientific and clinical experts, manage post-market studies, and provide regional medical meeting input for Becton, Dickinson's medical device portfolio.
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Global Scientific Communications Lead (m/f/d)
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Grünenthal Group
Lisboa, Lisbon, Portugal
16d
Own and evolve the global scientific communications strategy for early pipeline and commercialized assets, translating clinical evidence into clear scientific narratives to support medical strategy and launch readiness.
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Medical Lead, Hepatology
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Gsk
Worli, Maharashtra, India
16d
Develop strategy and deliver high-quality scientific non-promotional materials for Hepatology (Chronic Hepatitis B & MASH) to support brand strategy and evidence generation.
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Global Regulatory Strategy Lead
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Boehringer Ingelheim
Biberach an der Riß, BW, DE
16d
Develop and lead global strategic regulatory guidance and leadership throughout the product lifecycle for assigned Inflammation projects.
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Associate Director II, CReW
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AstraZeneca
KA, IN
16d
Provide strategic leadership and communications expertise to clinical drug programs, authoring complex clinical-regulatory documents and leading submission strategies.
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Regulatory Affairs Fellow (12 months)
Vrtx
Paddington, United Kingdom
16d
Develop regulatory strategies for development and commercialization of pharmaceutical programs and marketed products.
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Head of Regulatory Information Management
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GE HealthCare
KA, IN
16d
Lead the strategy, governance, and operating model for Regulatory Information Management (RIM) systems and data to ensure compliant, scalable business processes in life sciences.
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Associate Medical Director – Acute Therapies (w/m/d)
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Vantive
Remote
16d
Define medical strategy for innovative acute therapies (CRRT, blood purification, CO₂ removal, anticoagulation) across EMEA and translate clinical evidence into practical guidance for healthcare professionals.
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Sotyktu AM
Bristolmyerssquibb
Guangzhou - CN
16d
Lead regional business development and compliance for Sotyktu (an immunology drug), driving standardized treatment and patient management for psoriasis and other immune diseases.
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Manager, Global Regulatory Strategy
Sarepta
Cambridge, MA, US
$116k–$145k
16d
Regulatory strategy lead supporting clinical trial and registration activities for medicinal products across assigned markets.
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Associate Director, CMC Regulatory Science - UK
ModernaTX
London - England
16d
Lead CMC regulatory strategy for UK-manufactured and UK-licensed mRNA products from development through commercialization and post-approval lifecycle.
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Director, Responsible Business Reporting & Communications
Gilead
United States - California - Foster City
$210k–$272k
16d
Lead Responsible Business reporting and manage communications delivery across the Responsible Business and Corporate Responsibility portfolios.
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Director, Medical Affairs – Molecular Diagnostics
Abbott
United States - Illinois - Des Plaines
16d
Provide medical leadership for the development, regulatory approval, commercialization, and lifecycle management of Abbott Molecular's global diagnostic portfolio.
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