Medical Writing
734 open positions
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MA/MI Content Management & System Specialist EversanaPune, MH, in 18d Manage Medical Affairs and Medical Information (MA/MI) content, systems, and data to ensure accuracy, compliance, and accessibility for dedicated clients.
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2027 Future Talent Program - U.S. Medical Affairs - Payer & Health Systems - Intern MsdRemote $40k–$40k18d Internship role supporting US Medical Affairs, Payer & Health Systems by developing scientific engagement priorities, sharing insights with stakeholders, and updating field engagement plans based on regulatory and competitor data.
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Manager, Core Labeling Strategy ViatrisWashington, District of Columbia, USA $78k–$78k18d Develop, maintain, and implement global regulatory labeling (Product Information, CCDS, USPI, EU SmPC) for existing and new pharmaceutical products to ensure compliance with regulatory requirements.
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MR-GUGY-济南 AstraZenecaChina 18d Develop and execute pharmaceutical product promotion plans and communicate product information to medical professionals to support rational product use.
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Medical Affairs Associate↗ Blackmores GroupSurry Hills, NSW, AU 18d Assess promotional material for scientific accuracy and regulatory compliance, evaluate clinical evidence to substantiate health claims, and provide scientific/regulatory input for product development.
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Publication Coordinator SpringernatureTokyo 18d Manage the manuscript development and publication process for medical and pharmaceutical journals, serving as the primary liaison between authors, clients, and editorial offices.
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Regulatory Project Manager, Strategy - CMC RA Small Molecules Mature Products GskRemote 18d Provide CMC regulatory support for a portfolio of marketed small molecule drug substances and products to ensure global supply continuity and compliance.
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Global Labelling Lead IconRemote 18d Shape and implement strategic regulatory labelling plans for the development and approval of innovative treatments within Plasma derived therapies.
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Medical Writer↗ Kps LifeRemote 18d Create and review regulatory submission documents for clinical research, including clinical study reports, protocols, and safety/efficacy summaries.
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Regulatory Affairs Specialist Agardh Recruitment & Consulting ABVellinge, Sweden 19d Manage regulatory submissions and lifecycle activities for a generic pharmaceutical portfolio across European markets.
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Head of Representative Office (Belarus) AbbVieMinsk, Minsk Region, by 19d Senior country leader accountable for the compliant operation, performance, and cross-functional coordination of the company's business in Belarus, integrating strategy, external engagement, and governance.
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Director, Medical Affairs – Molecular Diagnostics↗ AbbottDes Plaines, IL, US 19d Provide medical leadership for the development, regulatory approval, commercialization, and lifecycle management of Abbott Molecular's global molecular diagnostics portfolio.
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Medical Affairs Lead CoMindRemote, US 19d Bridge clinical science and customers/academic partners for a non-invasive neuromonitoring technology company.
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Senior Manager 1, Submission Management BristolmyerssquibbWarsaw-WeWork-PL $251k–$251k19d Lead end-to-end regulatory submission strategies and production for US IND and marketing dossiers for global health authorities.
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Senior Event Manager (m/w/d)↗ Aristo Pharma GMBHBerlin, BE, DE 19d Conception, planning, and execution of complex scientific events to facilitate professional exchange and support the pharmaceutical company's growth.
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Regulatory Affairs Executive Pasona Singapore Pte. Ltd.Singapore $54k–$54k20d Manage the life cycle of existing product portfolios and prepare registration dossiers to obtain regulatory approvals in Singapore and Malaysia.
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Responsable Affaires Pharmaceutiques senior SobiParis, IDF, fr 22d Senior Pharmaceutical Affairs Manager responsible for regulatory, quality, and distribution activities for a pharmaceutical portfolio.
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Senior Medical Writer↗ Ashfield MedcommsRemote 22d Senior Medical Writer creating scientific publications (manuscripts, abstracts, posters, oral presentations) and patient-focused content for Oncology products.
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Senior Medical Writer↗ Nucleus GlobalRemote 22d Senior Medical Writer developing scientific expertise in assigned therapeutic areas to create technical materials for medical affairs teams.
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Scientific Relations Project Manager↗ TfsMadrid, MD, ES 22d Coordinate expert meetings and manage stakeholder engagement for a global pharmaceutical sponsor within the healthcare industry.
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サRegulatory Labeling Manager↗ サイネオス・ヘルスRemote 22d Develop, maintain, and oversee labeling content for mature pharmaceutical products, ensuring compliance with global regulations and internal governance.
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Regulatory Labeling Manager↗ Syneos HealthDesde casa, AR 22d Develop, maintain, and oversee labeling content for mature pharmaceutical products, ensuring compliance with global regulatory requirements and internal governance.
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Rheumatology Lead, Global and US Immunology Medical Affairs.↗ Eli LillyIndianapolis, IN, US 22d Lead global and US medical affairs strategy for Lilly's rheumatology portfolio, driving 10-year plans, evidence generation, and lifecycle management for marketed and late-phase assets.
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Sr. Corporate Communications Manager, Product Communications NeurocrineUS CA San Diego $149k–$149k22d Develops and shapes integrated corporate and product communications strategies and leads implementation of communications plans for assigned brands and therapeutic areas.
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Manager, Nonclinical Writing AlnylamUnited States 22d Lead nonclinical writing assignments and document review processes for early development and late-stage programs to support global regulatory filings.
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Senior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite) MedtronicFridley, Minnesota, United States of America $106k–$106k22d Lead the development of clinical, scientific, and regulatory documentation to support the global clinical development of neurovascular therapies for stroke and other conditions.
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US Transplantation Medical Publications Lead SanofiMorristown, NJ 22d Lead strategic development, oversight, and delivery of US Transplantation medical publications to ensure clear scientific communication of Sanofi data.
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Business Consultant - Medical Content VeevaRemote $70k–$70k22d Lead project workstreams to transform how Life Sciences companies work with Technology, Data, and AI, focusing on reshaping operating models and driving organizational change within the Vault Medical suite.
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