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Healthcare
› Medical Writing
Medical Writing
733 open positions
Senior Manager, Publications
AbbVie
North Chicago, IL, us
23d
Lead Publications Teams to execute scientific publication plans (clinical manuscripts, abstracts, posters, oral presentations) for assigned assets, ensuring alignment with strategic communication objectives.
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Director, State Government Affairs
AbbVie
North Chicago, IL, us
23d
Strategic leader responsible for developing and executing lobbying and advocacy strategies to shape state legislative and regulatory environments in support of AbbVie's business and policy objectives.
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Medical Writer Supervisor
Omnicomhealth
Remedy Edge - Barcelona
23d
Developing and supervising scientific content including slide decks, monographs, promotional materials, abstracts, and congress reports for healthcare clients.
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2027 Future Talent Program –Global Labeling Strategy - Intern
Msd
USA - Pennsylvania - North Wales (Upper Gwynedd)
$39k–$39k
24d
Drafting and revising labeling documents for medicine and vaccine products globally.
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Manager Evidence Synthesis
Sanofi
Hyderabad
24d
Manage evidence synthesis projects to generate health economics and value-based evidence for global and US market access strategies.
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TAM Hematología
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Servier
Madrid, MD, ES
24d
Define and lead medical strategic and operational activities for the Hematology therapeutic area.
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Associate Director, Regulatory Submission Management
Gilead
United States - California - Foster City
24d
Lead global regulatory submission planning and execution for complex biopharma programs, ensuring seamless delivery of marketing applications across multiple regions.
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Senior Global Medical Affairs Lead MASH
AstraZeneca
US - Boston - MA
24d
Senior Global Medical Affairs Leader shaping global medical strategies and evidence generation for MASH (Metabolic dysfunction-associated steatohepatitis) therapies within the Weight Management area.
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National Director, US Field Medical Cardiomyopathy
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Bristol Myers Squibb
Remote, US
24d
Leading a national team of Field Medical professionals (RADs, RDs, MSLs) to drive scientific exchange, support clinical trials, and facilitate patient access for Mavacamten and other Cardiovascular medicines.
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Senior Program Manager (SPM) - Mastocytosis
Sanofi
Cambridge, MA
24d
Drive business-related initiatives and lifecycle management for the Mastocytosis Therapeutic Area, serving as an operational partner to the Medical Program Lead and Global Medical Team.
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サ
Sponsor Dedicated - Regulatory Labeling Manager
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サイネオス・ヘルス
Remote
24d
Develop, maintain, and oversee labeling content for mature pharmaceutical products, authoring and updating documents in response to safety updates and regulatory requirements.
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Senior Medical Director - Biologics
AstraZeneca
US - Wilmington - DE
$244k–$244k
24d
US medical leadership for tezepelumab in severe asthma, chronic rhinosinusitis, eosinophilic esophagitis, and COPD, driving scientific strategy, evidence generation, and external engagement.
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Regulatory Project Manager
Iqvia
Durham, North Carolina, United States of America
$97k–$97k
24d
Support global development programs by translating regulatory strategy into executable plans and managing milestones, timelines, and deliverables across early- and late-stage stages.
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Global Medical Affairs Lead, PDT Immunology (Director)
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Takeda Pharmaceuticals
Cambridge, MA, US
24d
Co-lead development and execution of a multi-year global medical strategy for the PDT immunoglobulin portfolio, focusing on primary immunodeficiency (PID), secondary immunodeficiency (SID), and chronic inflammatory demyelinating polyneuropathy (CIDP).
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MINS (Medical Information /Nominated Signatory) Specialist (Fixed Term)
AstraZeneca
South Korea - Seoul, KR
24d
Deliver medical information on AstraZeneca products to healthcare professionals and internal customers, while reviewing and validating promotional and non-promotional materials for regulatory compliance.
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Associate Program Manager III
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Syneos Health Commercial Solutions
Buenos Aires, B, AR
24d
Create high-quality program materials and customer deliverables to make Life Science organizations more effective in complex specialty markets.
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Associate Program Manager III
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サイネオス・ヘルス
Buenos Aires, B, AR
24d
Create high-quality program materials and customer deliverables to make Life Science organizations more effective in complex specialty markets.
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Medical Writing Manager (Hybrid)
Vrtx
Boston, MA
$120k–$120k
24d
Lead Medical Writing Scientist preparing moderately complex clinical and regulatory documents for clinical studies.
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Senior Medical Writer
Omnicomhealth
Remedy Edge - Barcelona
24d
Develop scientifically rigorous and creatively engaging communication materials supporting clients' medical and promotional strategies.
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Senior Medical Editor
Omnicomhealth
Remedy Edge - Barcelona
24d
Ensures exceptional quality control across medical and scientific content, leading editorial excellence, process development, and proper referencing for healthcare clients.
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Medical Writer Assitant (Trainee)
Omnicomhealth
Remedy Edge - Barcelona
24d
Support medical strategy and scientific content creation for healthcare clients.
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Healthcare Innovation Manager
AbbVie
Bratislava, Bratislava Region, sk
24d
Lead compliant healthcare innovation collaborations with external stakeholders in CZ & SK to identify unmet needs and deliver measurable improvements in patient care.
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US Senior Medical Director, Autoimmune T1D
Sanofi
Morristown, NJ
25d
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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Regional Technical Manager Ruminants
Msd
HUN - Central Hungary - Budapest (Millennium Gardens)
25d
Regional Technical Manager providing scientific, veterinary, and regulatory expertise to support commercial objectives, customer interactions, and KOL engagement in the ruminants sector.
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Regional Medical Advisor
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Abbott
WB, IN
25d
Provides scientific and medical support to Abbott customers in the field, ensuring compliance with regulations while advancing scientific credibility with opinion leaders.
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Government Affairs & Patient Advocacy Manager
AstraZeneca
Thailand - Bangkok
25d
Lead external engagement to influence public policy and patient access to innovative medicines by connecting scientific progress to policy realities.
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Manager - Submission Management, Established Products
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Merck Kgaa
KA, IN
25d
Lead the Submission Management sub-team within Global Regulatory Affairs to ensure high-quality, compliant, and timely regulatory submissions for medicines and devices.
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顧問類-專員/資深專員(生技產業)
PwC
Taipei, TW
25d
Researching and writing reports on biotech/medical industry trends and planning/executing professional lectures and international forums.
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Multilingual Medical Information Specialist - Pharmacist (French/English)
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ProPharma Group
Remote
25d
Provide medical and safety information responses, document adverse events, and translate documents for pharmaceutical clients via phone, email, and web.
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Medical Advisor, Ideation & Portfolio Development
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Dr. Reddy's Laboratories
MH, IN
25d
Provide scientific and clinical leadership for identifying, evaluating, and developing new pharmaceutical product opportunities across therapeutic areas.
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Senior Medical Writer
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BGBx
Toronto, ON, CA
$100k–$100k
25d
Develops scientifically accurate, strategically aligned, and impactful medical content for pharmaceutical and life science clients from initiation through completion.
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Senior Medical Copywriter/Editor
Accenture
Toronto, 40 King St W., Corp
$64k–$64k
25d
Senior Medical Copywriter/Editor responsible for developing compliant pharmaceutical marketing content for patients and healthcare providers.
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Regulatory Affairs Associate Director - EU Regulatory Lead - FSP Client Dedicated
Thermofisher
Remote, Belgium
25d
Lead EU regulatory strategy and submissions for a dedicated pharmaceutical client, guiding product development from preclinical stages through registration and commercialization.
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Medical Director (m/w/x)
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Doctorflix
Berlin, BE, DE
25d
Lead the medical content catalog and format development for a major CME learning platform, ensuring evidence-based medical knowledge reaches thousands of doctors in Germany.
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Senior Labeling Hub Manager
Viatris
Lisbon, Lisbon, Portugal
25d
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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Medical Information Specialist
Praxisprecisionmedicines
Remote
$145k–$145k
25d
Primary human expert for complex Medical Information escalations, ensuring AI-generated responses remain accurate and balanced while building scalable scientific content libraries.
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Senior Manager RA US Advertising and Promotion - Hybrid
AbbVie
North Chicago, IL, us
25d
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
25d
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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Medical Director Romania
AbbVie
Bucharest, Bucharest, ro
25d
Lead the affiliate Medical department in Romania, executing Medical Affairs strategies, managing pharmacovigilance, and ensuring compliance with patient safety and regulatory standards.
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Regulatory Affairs Specialist/Regulatory Scientist - FSP
Thermofisher
Remote, Belgium
26d
Develop and execute global and regional regulatory strategies for pharmaceutical programs across development and post-approval maintenance.
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Senior Manager, Commercial Training and Development
Alnylam
Remote
$147k–$147k
26d
Develop and implement capability-building strategies and learning solutions to drive measurable field performance and business outcomes for the TTR Franchise.
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Director, BPM Evidence Publications CVRM
AstraZeneca
US - Gaithersburg - MD
$164k–$247k
26d
Develop and execute strategic publication plans for global clinical registration studies and non-clinical trial sources including HEOR, epidemiology, real-world evidence, payer, and non-interventional studies.
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Partnership Manager Australia (Medical Doctor)
Amboss
Remote
26d
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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Director, Publications
Regeneron
SLEEPY HOLLOW, US
$183k–$183k
26d
Lead strategic direction and operational performance of publication plans for assigned therapeutic assets, collaborating with authors, Medical Affairs partners, and external agencies.
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Medical Editor
Klick
Toronto, Ontario, ca
$70k–$80k
26d
Ensures scientific accuracy, clarity, and regulatory compliance for healthcare professional and patient-facing marketing materials.
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Associated Director International Learning Immunology Gastro Portfolio
AbbVie
Mettawa, IL, us
26d
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
26d
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
27d
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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Assoc Director - Publishing
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Novo Nordisk, Inc.
KA, IN
27d
Lead global publishing activities and eCTD submission structures to ensure regulatory compliance for Novo Nordisk's medicines.
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Senior Medical Advisor Respiratory
Sanofi
Seoul
27d
Execute non-promotional medical and scientific strategy for the Respiratory & Rhinology (Dupixent) portfolio, partnering with franchise leads and stakeholders to raise standards of care and change clinical practice.
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