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Healthcare
› Medical Writing
Medical Writing
705 open positions
[MA] Senior Medical Affairs Scientist Manager - Amyloidosis (Cardiology)
Pfizer
Japan - Tokyo
2mo
Lead the Amyloidosis team in Japan, acting as the primary scientific and medical point of contact for cardiologists, heart failure specialists, and multidisciplinary centers to establish Pfizer as a trusted partner in the amyloidosis treatment landscape.
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Assistant Manager, GRA Business Process
Viatris
Northern Cross, Dublin, Ireland
2mo
Develop, optimize, and implement compliant business processes and documentation (SOPs, WIs, JAs, QRGs) for Global Regulatory Affairs to ensure consistent execution across global teams.
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Manager, Medical Writing FSP
Thermofisher
Remote, India
2mo
Manage a team of Medical Writers to ensure operational excellence, resource planning, and delivery of high-quality regulatory and clinical documents.
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Senior Director, Compliance Business Partner
Madrigalpharma
PA - Conshohocken - Office, US
$254k–$254k
2mo
Senior Director providing risk-based compliance guidance and oversight for commercial activities, healthcare professional engagements, and patient support programs in a biopharmaceutical company.
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Director, Corporate Communications
Xenon
Boston
2mo
Develop and execute corporate, investor, executive, and R&D communications strategies to promote Xenon Pharmaceuticals' reputation and pipeline.
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Scientific Director
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Open Health
Remote
2mo
Lead multiple client projects simultaneously as the medical expert, developing high-quality medical and commercial content to support strategic product positioning.
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Medical Editor
Eversana
Overland Park, KS, us
2mo
Develops and reviews medical/scientific content for healthcare products, ensuring scientific accuracy, regulatory compliance, and editorial excellence for healthcare professionals and patients.
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Head of US Regulatory Affairs Advertising and Promotion, Global Regulatory Affairs
Viatris
Washington, District of Columbia, USA
$151k–$151k
2mo
Senior leadership role ensuring US advertising and promotion compliance for pharmaceutical products while providing strategic regulatory guidance to enable business growth.
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Medical writer
Ctc Clinical Trial Consultants AB
Uppsala, Sweden
2mo
Writing and quality-checking regulatory documents, primarily clinical study protocols and reports, for pharmaceutical and medtech industry clients.
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Senior Medical Writer – Client Aligned (FSP)
Thermofisher
Remote, United Kingdom
2mo
Develop high-quality clinical and regulatory documents for a client in the FSP space, ensuring alignment with regulatory guidelines and company standards.
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Regional Submission Planner Senior Specialist
Msd
CZE - Central Bohemian - Prague (Five)
2mo
Plan, coordinate, and execute regulatory submissions for pharmaceutical products across the EU and EEMEA regions to ensure timely approval by Health Authorities.
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ED/VP Medical Science & Strategy - Metabolic
Thermofisher
Beijing, China
2mo
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 Advisor, Hematology
AbbVie
Seoul, Seoul, kr
2mo
Lead medical affairs strategy and team management for hematology oncology products, generating scientific evidence to support healthcare professionals and patients.
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Senior Manager, US Medical Affairs
Dynetherapeutics
Waltham, MA
$165k–$165k
3mo
Execute US Medical Affairs strategy and launch readiness for Duchenne Muscular Dystrophy (DMD) therapeutic programs.
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Medical Evidence & Project Advisor/Manager (all gender) - in Teilzeit (15h), befristet auf 1 Jahr
AbbVie
Remote
3mo
Managing strategic evidence planning and operational project management for non-interventional studies (NIS) and physician-initiated studies (IIS) within Medical Affairs.
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Manager, Medical Education, SEA & SA
↗
Zimmer Biomet
40, TH
3mo
Define and drive medical training and education strategy for Southeast Asia and South Asia regions, tailoring programs for Healthcare Professionals (HCPs) and developing faculty.
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Global Medical Advisor - Rescue Treatments
Peopleservices
GB Cambridge
3mo
Global medical authority leading strategy and execution for opioid agonist treatment and overdose management rescue therapies.
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Assistant Regulatory Manager/Senior Regulatory Executive, Complementary Health Products Branch
Sggovterp
BIOPOLIS (HELIOS BUILDING)
3mo
Conduct post-market compliance checks for complementary health and cosmetic products, manage stakeholder enquiries, and develop digital training resources.
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Product Line Manager II - Medical Components
Nordsonhcm
USA - New Hampshire - Salem
3mo
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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[MA] Dermatology, MAS(Field) Manager
Pfizer
Japan - Tokyo
3mo
Serve as the medical scientific point of contact for HCPs, medical societies, regulators, and academia in dermatology, managing scientific exchanges, UMRs, and medical plans.
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Medical, Legal and Regulatory (MLR) Coordinator
Eversana
Overland Park, KS, us
3mo
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 Writing Lead
Biibhr
Beijing, China
3mo
Lead author of regulatory and scientific documentation for China, managing content collection and vendor work to ensure compliance with ICH guidelines and local regulations.
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Medical Writer / Medical Reviewer Consultant – Oncology (Ovarian Cancer)
ClinChoice
Remote
3mo
Develop, review, and deliver high-quality scientific and medical content for ovarian cancer therapies, ensuring accuracy and regulatory compliance.
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Associate Director, Medical Affairs-Strategic Business Planning & Execution,
Regeneron
SLEEPY HOLLOW
$157k–$157k
3mo
Project management support for Global Medical Affairs Head and Medical Directors within the Neurology Franchise, driving execution of medical tactics and overseeing studies.
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Senior Regulatory Medical Writer, Client-embedded, FSP
Thermofisher
Remote
$105k–$105k
3mo
Senior Medical Writer authoring clinical and preclinical regulatory documents for internal and external clients to ensure operational excellence and compliance.
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Korean Linguist - (Pharma/CRO/Lifescience)
Welo Global
South Korea
3mo
Managing translation and copy-editing tasks for pharmaceutical, CRO, and medical device organizations to ensure regulator-ready linguistic deliverables for clinical trials, pharmacovigilance, and regulatory affairs.
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Associate Director, Medical Training (Pipeline)
Xenon
Boston
3mo
Lead strategy, development, and execution of medical training programs for the company's neuroscience pipeline (epilepsy, MDD, bipolar depression) to ensure internal teams communicate science and evidence accurately.
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VP Global Pharma & Healthcare
Jas
United States of America, Georgia, Atlanta
3mo
Senior executive responsible for strategic leadership, growth, and operational excellence of global supply chain verticals and key account development.
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Senior Manager, Regulatory Affairs CMC
Viatris
Northern Cross, Dublin, Ireland
3mo
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
↗
Eli Lilly and Company
Bad Homburg, Hesse, Germany
3mo
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
3mo
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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Associate Director, CMC Regulatory Affairs, International
ModernaTX
London - England
3mo
Lead global CMC regulatory strategies and submissions for Moderna's mRNA medicines, ensuring compliance with international health authority requirements.
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Senior Director, Mavacamten Medical Product Lead
Bristolmyerssquibb
Princeton - NJ - US
$229k–$229k
3mo
Strategic leadership of global medical affairs and evidence generation for Mavacamten (Camzyos®) in hypertrophic cardiomyopathy.
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Medical (Science) Director - Rare Blood Disorders/Hematology
Roche
South San Francisco
$173k–$173k
3mo
Provide clinical and scientific leadership for medical affairs activities in rare blood disorders/hematology, generating evidence for practitioners, patients, and payers.
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Sr Manager, Medical Affairs - Liver
Gilead
Japan - Tokyo
3mo
Lead strategic data generation and medical programs for liver disease therapies in Japan, including advisory boards, educational initiatives, and launch planning.
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Senior Medical Writer
Thermofisher
Shanghai, China
3mo
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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Medical Writer
Lumanity
London, London, England, United Kingdom
3mo
Producing high-quality medical communications content including manuscripts, outlines, symposia, and training materials for life sciences clients.
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Principal, Medical Affairs Innovation
Bdx
USA NJ - Franklin Lakes
3mo
Lead clinical assessment and strategy for innovation projects in specimen management, generating and communicating clinical evidence to support product development and regulatory submissions.
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Medical Editor
Synchrony Group, LLC
West Chester, West Chester, Pennsylvania, United States
3mo
Ensuring editorial quality, accuracy, and consistency for medical communications content including slide decks, scripts, and digital materials.
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Advisor, Medical
AbbVie
Shanghai, Shanghai, cn
3mo
Develop and execute medical strategies, evidence generation plans, and scientific communications for pharmaceutical brands and therapeutic areas.
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Senior Medical Writer
Icon
Remote
3mo
Leading the development of high-quality regulatory and clinical documents to support clients' submissions to regulatory authorities.
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Medical Affairs Manager (m/w/d) Amyloidosis
AstraZeneca
Germany - Hamburg
3mo
Develop and execute medical strategy for amyloidosis treatments, collaborating with cross-functional teams, scientific societies, and regulators to confirm drug efficacy and support market access.
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Medical manager
Biibhr
Tokyo, Japan
3mo
Provide scientific and educational medical support for therapeutic areas and Biogen products to cross-functional teams within the company.
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Medical Information Specialist with French
Thermofisher
Sofia, Bulgaria
3mo
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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Manager, Regulatory Affairs, Advertising & Promotion
Regeneron
SLEEPY HOLLOW, US
$129k–$129k
3mo
Manage US regulatory activities for advertising and promotion of marketed pharmaceutical products, ensuring compliance with FDA regulations and supporting commercial objectives.
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Regulatory Affairs Manager
↗
Cencora
40, TH
3mo
Managing regulatory affairs for the lifecycle of pharmaceutical products, including approvals, variations, and compliance with local health authorities.
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Regulatory Affairs CMC Associate II
Iovancebiotherapeutics
Remote
$120k–$120k
3mo
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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Head of Medical Information (Director/Senior Director) – Medical Affairs
Vorbiopharma
Boston
$220k–$220k
4mo
Lead the Medical Information (MI) function to build operational infrastructure, ensure regulatory compliance, and manage scientific responses for a dual BAFF/APRIL inhibitor treating autoimmune diseases.
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CMC Project Manager
Icon
US, Blue Bell (ICON)
4mo
Design and analyze clinical trials, interpret complex medical data, and oversee regulatory affairs delivery to advance innovative treatments.
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Responsable Médical Aire Thérapeutique, Gastroentérologie
AbbVie
Boulogne-Billancourt, fr
4mo
Define and implement medical strategy, development plans, and publication plans for gastroenterology therapeutic area products in alignment with global strategy.
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