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Healthcare
› Medical Writing
Medical Writing
1,313 open positions
CMC Asset Lead, Nephrology
Biibhr
Cambridge, MA, US
$204k
3mo
Lead the commercialization and life cycle management of a critical nephrology asset in clinical development, overseeing strategy, launch planning, and project financials for multiple indications including three Phase 3 studies.
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Pharmazeut im Praktikum - Medical Affairs (w/m/d)
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Stada Group
Bad Vilbel, Hesse, Germany
3mo
Supporting Medical Managers in product and indication areas by creating scientifically compliant materials, answering medical inquiries, and evaluating innovative product ideas.
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Senior Translation Project Manager
Icon
Singapore, Singapore
3mo
Lead planning, coordination, and delivery of clinical document translations in a highly regulated global environment, integrating AI-enabled translation technologies.
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Sr Manager, Medical Information
Gilead
United States - California - Foster City
$169k–$219k
3mo
Provides strategic and scientific leadership for the development and delivery of high-quality medical information for Gilead products, serving as a Therapeutic Area subject matter expert.
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【Alexion Japan】Head of Medical Affairs, Rare Bone & Endocrine Disorders, Rare Tumours
AstraZeneca
Minato-ku, Tokyo, Japan
3mo
Provide strategic leadership for Alexion's Rare Bone & Endocrine Disorders and Rare Tumours portfolio, setting evidence-based medical standards and developing local strategies in Japan.
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Director, RA Global Regulatory Strategy
AbbVie
North Chicago, IL, us
4mo
Develops and implements global regulatory strategies to secure and maintain market approval for pharmaceutical products in assigned therapeutic areas.
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(Junior) Market Access & HTA-Manager / (Junior) Berater (m/w/d)
IGES GmbH
Remote
4mo
Creating AMNOG and future EU-HTA dossiers and supporting benefit assessment processes for pharmaceutical and medical device companies.
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FSP Principal Medical Writer (Regulatory) - Client-Dedicated
Thermofisher
Remote
4mo
Lead medical writer providing high-quality scientific writing, planning, coordination, and delivery of clinical study reports, protocols, and regulatory documents (IBs, INDs, MAAs) for internal and external clients in the pharmaceutical/CRO industry.
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Global Patient Access Strategy Lead (Sr. Manager)
Takeda
USA - MA - Cambridge - Kendall Square - 500
$178k–$245k
4mo
Lead development and advancement of Global Patient Access (GPA) strategies across programs, ensuring alignment with enterprise priorities, regulatory requirements, and product lifecycle needs.
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Associate Principal, Patient-Centered Research
Iqvia
Durham, North Carolina, United States of America
$111k
4mo
Overseeing a portfolio of consulting, scientific, and analytic projects to design and execute patient-centered research for new medicine development and commercialization.
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Senior Manager, HEOR - Endocrinology
Neurocrine
US CA San Diego
$155k–$211k
4mo
Designs and implements HEOR projects to establish disease prevalence, burden of disease, and health outcomes to inform commercial strategy, value assessment, and market access.
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Associate General Counsel, R&D Innovation Legal
AbbVie
Washington, DC, us
4mo
Provide strategic legal counsel to AbbVie's R&D organization on regulatory filings, agency engagements, and pipeline development issues.
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Associate General Counsel, R&D Innovation Legal
AbbVie
North Chicago, IL, us
4mo
Provide strategic legal counsel to AbbVie's R&D organization on regulatory filings, agency engagements, and pipeline development issues.
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Director, Clinical Regulatory Writing (Program Lead)
AstraZeneca
Spain - Barcelona
4mo
Provides expert communications leadership across clinical programs, driving collaboration and growth within Clinical Regulatory Writing to achieve successful submissions and approvals.
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Executive Director, Global Head of Medical AI/Digital Strategy & Enablement
AstraZeneca
US - Gaithersburg - MD
$283k–$425k
4mo
Define multi-year AI/digital strategy and operating models to enable 3,000+ medical colleagues to use GenAI and data tools for scientific engagement and evidence-informed decisions.
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Clinical and Medical Internship - Pharmaziepraktikum* (f/m/d)
Pg
SCHWALBACH GO & TECH CENTER
€31k
4mo
Support cross-functional projects spanning Rx, OTC, medical device, and food supplement portfolios by preparing competitive benchmark analyses, conducting literature searches, and assisting in clinical trial document preparation.
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Artwork Coordinator
Viatris
Lisbon, Lisbon, Portugal
4mo
Coordinate artwork creation, approval, and implementation for pharmaceutical products to ensure compliance with regulatory and business requirements.
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Head of Global Medical Affairs
Praxisprecisionmedicines
Remote
4mo
Building and leading the global medical affairs function to support the development and commercialization of a neuroscience pipeline.
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Medical Writer Scientific Communications
Prime
Remote
4mo
Develop high-quality medical communications materials including abstracts, posters, manuscripts, slide decks, and presentations for global healthcare partners.
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Director, Medical Affairs Analytics & Planning - International Medical Affairs
AbbVie
Mettawa, IL, us
4mo
Leads integrated analytics, planning, and insight-generation capabilities across international affiliates to enable data-informed decision-making for Medical Affairs leadership and field effectiveness.
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Head of International Policy
AbbVie
North Chicago, IL, us
4mo
Lead analysis of international public policy developments and develop strategies to support AbbVie's engagement with policymakers to advance business goals.
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Director, Corporate Communications
Xenon
Boston
4mo
Develop and execute corporate, investor, executive, and R&D communications strategies to promote Xenon Pharmaceuticals' reputation and pipeline.
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[MA] Senior Medical Affairs Scientist Manager - Amyloidosis (Cardiology)
Pfizer
Japan - Tokyo
4mo
Lead the Amyloidosis team in Japan as the medical and scientific point of contact for cardiologists, heart failure specialists, and multidisciplinary centers, bridging clinical insights with Medical Affairs excellence to establish Pfizer as a trusted…
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Director, Global Submission Management
Vrtx
Boston, MA
$190k
4mo
Strategic oversight and execution of a global portfolio of regulatory submissions across development and lifecycle programs to enable product registrations.
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Head of US Regulatory Affairs Advertising and Promotion, Global Regulatory Affairs
Viatris
Washington, District of Columbia, USA
$151k–$314k
4mo
Senior leadership role ensuring US advertising and promotion compliance for pharmaceutical products while enabling compliant business growth.
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Medical writer
Ctc Clinical Trial Consultants AB
Uppsala, Sweden
4mo
Writing and quality-checking regulatory documents, primarily clinical study protocols and reports, for pharmaceutical and medtech industry clients.
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ED/VP Medical Science & Strategy - Metabolic
Thermofisher
Beijing, China
4mo
Lead medical science and strategy for metabolic disease clinical research, supporting sales proposals, bid defenses, and client advisory boards while driving business growth in the PPD clinical research portfolio.
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Medical Manager (CVRM)
AstraZeneca
Poland - Warsaw
4mo
Define medical strategy and execute medical activities for the Cardiovascular-Renal-Metabolic (CVRM) portfolio to support product launches and ensure therapies reach patients.
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Senior Manager, US Medical Affairs
Dynetherapeutics
Waltham, MA
$165k
4mo
Execute US Medical Affairs strategy and launch readiness for Duchenne Muscular Dystrophy (DMD) therapeutic programs.
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Global Medical Advisor - Rescue Treatments
Peopleservices
GB Cambridge
4mo
Global medical authority leading strategy and execution for opioid agonist treatment and overdose management rescue therapies.
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Product Line Manager II - Medical Components
Nordsonhcm
USA - New Hampshire - Salem
4mo
Responsible for product planning and execution throughout the product lifecycle for medical components, partnering with sales, engineering, and regulatory teams to meet revenue and customer satisfaction goals.
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Medical, Legal and Regulatory (MLR) Coordinator
Eversana
Overland Park, KS, us
4mo
Coordinates end-to-end Medical, Legal, and Regulatory (MLR) review processes for healthcare marketing content to ensure compliance and accuracy before publication.
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Medical Writer / Medical Reviewer Consultant – Oncology (Ovarian Cancer)
ClinChoice
Remote
4mo
Develop, review, and deliver high-quality scientific and medical content for ovarian cancer therapies, ensuring accuracy and regulatory compliance.
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Senior Manager, Regulatory Affairs CMC
Viatris
Northern Cross, Dublin, Ireland
4mo
Senior Manager leading global CMC regulatory strategy, compliance, and submission planning for Upjohn's branded pharmaceutical portfolio.
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Director (m/w/d) Medical Affairs Allgemeinmedizin Cardiometabolic Health
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Eli Lilly and Company
Bad Homburg, Hesse, Germany
4mo
Strategic planning and execution of Medical Affairs activities for Cardiometabolic Health, focusing on Primary Care physicians to position the company as a scientific partner.
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Senior Medical Manager
Biibhr
Tokyo, Japan
4mo
Strategic architect and scientific leader building the medical function from the ground up for a new therapeutic area launch, shaping medical strategy and driving cross-functional activities.
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Medical Writer - PhD - Cardiovascular/Metabolic - Cincinnati
Medpace
Cincinnati, Ohio
4mo
Lead development of high-quality clinical and regulatory documents to support the safe and effective development of medical therapeutics.
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Senior Medical Writer
Thermofisher
Shanghai, China
4mo
Principal Medical Writer serving as primary author for clinical study reports, study protocols, and data summaries for internal and external clients.
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Sr Manager, Medical Affairs - Liver
Gilead
Japan - Tokyo
4mo
Lead strategic data generation and medical programs for liver disease therapies in Japan, including advisory boards, educational programs, and congress symposia.
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Medical Writer
Lumanity
London, London, England, United Kingdom
4mo
Producing high-quality medical communications content including manuscripts, outlines, symposia, and training materials for life sciences clients.
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Medical Editor
Synchrony Group, LLC
West Chester, West Chester, Pennsylvania, United States
5mo
Ensuring editorial quality, accuracy, and consistency for medical communications content including slide decks, scripts, and digital materials.
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Senior Medical Writer
Icon
Remote
5mo
Leading the development of high-quality regulatory and clinical documents to support clients' submissions to regulatory authorities.
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Medical manager
Biibhr
Tokyo, Japan
5mo
Provide scientific and educational medical support for therapeutic areas and Biogen products to cross-functional teams within the company.
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VP Global Medical Affairs & Clinical Operations (m/w/d)
Polymedics Innovations Gmbh
Kirchheim unter Teck
5mo
Leading global Medical Affairs and Clinical Operations to drive scientific strategy, market access, and product launch in new indications for a MedTech company.
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Medical Information Specialist with French
Thermofisher
Sofia, Bulgaria
5mo
Front-line specialist providing concise, accurate, and non-promotional medical information regarding medicinal products or devices to healthcare professionals and patients.
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Regulatory Affairs CMC Associate II
Iovancebiotherapeutics
Remote
$120k
5mo
Coordinate CMC submissions for clinical and commercial applications, managing planning, compilation, QC, and eCTD dossier preparation for tumor infiltrating lymphocyte (TIL) therapy products.
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English (US) to French (Canada) Linguist for Life Sciences (Pharmacovigilance)
Welo Global
Remote
5mo
Translate English (US) to French (Canada) medical and clinical content for global health and safety initiatives.
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Head of Global Regulatory Advertising and Promotion
Sobi
Waltham, MA, us
$260k–$290k
5mo
Leading global post-marketing regulatory activities for Sobi's pharmaceutical products, ensuring FDA compliance for promotional materials and managing the global review process.
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Vice President, US Medical Neurology
Roche
South San Francisco, US
5mo
Lead a strategic medical organization for the neurology portfolio, driving innovation, scientific leadership, and population health principles to improve patient outcomes.
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Medical Operations Manager
Amgen
India - Hyderabad
5mo
Manage and evolve Scientific Communications project management capabilities, driving process standardization, technology solution maintenance, and efficiency in medical content operations and publications.
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