Medical Writing
705 open positions
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Regulatory Affairs Specialist Agardh Recruitment & Consulting ABVellinge, Sweden 22d 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 23d 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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Gerente Medico↗ AbbottCiudad de México, DIF, MX 23d Lead the Medical Affairs function for a pharmaceutical affiliate, overseeing medical strategy, evidence generation, and compliance while supporting marketing and sales teams.
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Senior Event Manager (m/w/d)↗ Aristo Pharma GMBHBerlin, BE, DE 23d Conception, planning, and execution of complex scientific events to facilitate professional exchange and support the pharmaceutical company's growth.
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Senior Manager 1, Submission Management BristolmyerssquibbWarsaw-WeWork-PL $251k–$251k23d Lead end-to-end regulatory submission strategies and production for US IND and marketing dossiers for global health authorities.
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Medical Affairs Lead CoMindRemote, US 23d Bridge clinical science and customers/academic partners for a non-invasive neuromonitoring technology company.
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Manager Regulatory CMC Sciences (Injectables) ViatrisInverin, County Galway, Ireland 23d Develop and implement global CMC regulatory strategies for injectable products, ensuring compliance and managing lifecycle submissions.
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Regulatory Affairs Executive Pasona Singapore Pte. Ltd.Singapore $54k–$54k24d 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 25d Senior Pharmaceutical Affairs Manager responsible for regulatory, quality, and distribution activities for a pharmaceutical portfolio.
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Medicīnas konsultants/-e retajās slimībās– Latvija (jauktais/hibrīda darba režīms) AstraZenecaLatvia - Riga $48k–$72k26d Medical Advisor for rare diseases driving pre-launch excellence, practice change initiatives, and patient pathway optimization through scientific engagement and strategic partnerships.
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Regulatory Labeling Manager↗ Syneos HealthDesde casa, AR 26d Develop, maintain, and oversee labeling content for mature pharmaceutical products, ensuring compliance with global regulatory requirements and internal governance.
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Medical Writer Nucleus GlobalRemote 26d Develop scientific expertise in assigned therapeutic areas to create technical materials for medical communications.
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Senior Medical Writer Ashfield MedcommsRemote 26d Senior Medical Writer supporting a global pharmaceutical client's Oncology publications and medical affairs account, creating content for scientific publications, patient-focused materials, and presentations.
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ViiV Healthcare (GSK) North America Medical Director GskUSA - North Carolina - Durham 26d Lead product-specific medical strategy and scientific communications for ViiV HIV medicines in the US, aligning internal and external stakeholders to address unmet medical needs and support product lifecycle management.
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Regulatory Affairs - Regional Dossier Publisher MsdCZE - Central Bohemian - Prague (Five), CZ 26d Regional subject matter expert for regulatory submission publishing, managing dossier structures, file formats, and electronic transmissions to health authorities in EU and EEMEA.
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US Transplantation Medical Publications Lead SanofiMorristown, NJ 26d Lead strategic development, oversight, and delivery of US Transplantation medical publications to ensure clear scientific communication of Sanofi data.
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Scientific Relations Project Manager↗ TfsMadrid, MD, ES 26d Coordinate expert meetings and manage stakeholder engagement for a global pharmaceutical sponsor within the healthcare industry.
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Rheumatology Lead, Global and US Immunology Medical Affairs.↗ Eli LillyIndianapolis, IN, US 26d 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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サRegulatory Labeling Manager↗ サイネオス・ヘルスRemote 26d Develop, maintain, and oversee labeling content for mature pharmaceutical products, ensuring compliance with global regulations and internal governance.
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Senior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite) MedtronicFridley, Minnesota, United States of America $106k–$106k26d 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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Manager, Nonclinical Writing AlnylamUnited States 26d Lead nonclinical writing assignments and document review processes for early development and late-stage programs to support global regulatory filings.
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Sr. Corporate Communications Manager, Product Communications NeurocrineUS CA San Diego $149k–$149k26d 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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Business Consultant - Medical Content VeevaRemote $70k–$70k26d 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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Medical Writer Supervisor OmnicomhealthRemedy Edge - Barcelona 26d Developing and supervising scientific content including slide decks, monographs, promotional materials, abstracts, and congress reports for healthcare clients.
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IBU Medical Education Lead, Immunology 8036 Takeda Pharmaceuticals International AGSchweiz $169k–$169k27d Lead the execution of global medical education strategies and programs for immunology therapeutic areas across the International Business Unit (IBU) and Local Operating Companies.
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Senior Account Executive, Health Communications GCI HealthSingapore 27d Supporting the execution of scientific and health communication initiatives for pharmaceutical and biotech clients by developing high-quality scientific content and managing project timelines.
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TAM Hematología↗ ServierMadrid, MD, ES 27d Define and lead medical strategic and operational activities for the Hematology therapeutic area.
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Regulatory Project Manager IqviaDurham, North Carolina, United States of America $97k–$97k27d 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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サAssociate Program Manager III↗ サイネオス・ヘルスBuenos Aires, B, AR 27d Create high-quality program materials and customer deliverables to make Life Science organizations more effective in complex specialty markets.
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サSponsor Dedicated - Regulatory Labeling Manager↗ サイネオス・ヘルスRemote 27d 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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Associate Program Manager III↗ Syneos Health Commercial SolutionsBuenos Aires, B, AR 27d Create high-quality program materials and customer deliverables to make Life Science organizations more effective in complex specialty markets.
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Associate Director, Regulatory Submission Management GileadUnited States - California - Foster City 27d Lead global regulatory submission planning and execution for complex biopharma programs, ensuring seamless delivery of marketing applications across multiple regions.
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Global Medical Affairs Lead, PDT Immunology (Director)↗ Takeda PharmaceuticalsCambridge, MA, US 27d 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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Medical Writing Manager (Hybrid) VrtxBoston, MA $120k–$120k27d Lead Medical Writing Scientist preparing moderately complex clinical and regulatory documents for clinical studies.
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