Medical Writing
703 open positions
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Global Value Dossiers Writer - Global Health Economics team - Lisbon (hybrid/home-based)↗ IqviaOeiras, P11, PT 9d Consultant Medical Writer producing high-quality written content for Global Value Dossiers (GVDs), Health Technology Assessment (HTA) submissions, and Health Economic and Outcome Research (HEOR) study reports for pharmaceutical clients and payers.
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Advisor, MIDC AstraZenecaChina 9d Regional subject matter expert providing expert-level medical information, managing medical information processes, and leading team development within a pharmaceutical context.
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Senior Director, Medical Affairs Edwards2 Locations $209k–$209k9d Lead the Medical Affairs strategy for the Transcatheter Mitral & Tricuspid (TMTT) business unit to generate and disseminate evidence-based clinical practices for patients with cardiovascular disease.
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Associate Director, Regulatory Affairs MsdZAF - Gauteng - Midrand, ZA 9d Lead the Regulatory Affairs team to secure timely approvals and maintain optimal product positioning for medicines in South Africa and Sub-Saharan Africa.
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Signatory Lead↗ NovartisLondon, ENG, GB $68k–$126k9d Final medical signatory ensuring promotional and non-promotional materials comply with ABPI Code of Practice, regulations, and Novartis policies.
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サManager, FSP 360↗ サイネオス・ヘルスBuenos Aires, B, AR 9d Manager leading Functional Service Provider (FSP) partnerships to support drug development and commercialization for life sciences customers.
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Medical Writer BGBxRemote $70k–$70k9d Lead medical content development for pharmaceutical and life science clients, ensuring scientifically rigorous and strategically aligned deliverables.
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Associate Content Acquisition Manager WileyBeijing, CHN, CN 9d Identify and solicit topical content and prospective contributors for special issues in Health or Life Sciences, driving content growth and journal visibility.
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Scientific Projektmanager Kijimea (synformulas Gmbh)Gräfelfing/Munich 9d Drive regulatory strategy and international market access for innovative microbiota products at the intersection of R&D, Quality Assurance, and Regulatory Affairs.
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Medical Lead, Singapore & Distribution Markets and Medical Launch Lead, Asia AbbVieSingapore 9d Lead medical launch preparations and drive scientific exchange for Allergan Aesthetics portfolios across Asia markets, serving as a local representative for the Global Medical Office.
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Korean to English Medical Linguist The Language Doctors, Inc.Sydney, New South Wales 10d Translate Korean medical documents (patient records, medical reports) into English with accurate terminology and style consistency.
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Principal Associate, Regulatory Affairs CSL PlasmaMelbourne, Victoria 11d Develop regulatory strategies and manage product registrations and maintenance for prescription medicines in Australia and New Zealand, supporting new product applications and in-licensing opportunities.
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[MA] Vaccines Medical Affairs Scientist, Manager PfizerJapan - Tokyo 11d Serve as the primary medical scientific point of contact for Healthcare Professionals (HCPs), medical societies, regulators, and academia in Japan to establish clinical evidence and address unmet medical needs for vaccines.
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Hybrid Scientific Advisor Rare Disease (12 months fixed term) IpsenMelbourne, Victoria 12d Provide strategic and tactical medical expertise for Bylvay in paediatric hepatology/gastroenterology and rare cholestatic liver diseases, supporting evidence-based clinical decision-making and medical strategy.
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サSponsor Dedicated Regulatory Portfolio Snr. Regulatory Consultant (GRO RPSM) open to Spain, Portugal and UK location↗ サイネオス・ヘルスRemote 12d Senior Regulatory Consultant managing dedicated regulatory portfolios for pharmaceutical sponsors, supporting global regulatory affairs and submission strategies.
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Associate Director, PDS Communications, Product Development & External Manufacturing BristolmyerssquibbPrinceton - NJ - US $157k–$157k12d Develop and execute strategic internal and external communications for Product Development and External Manufacturing organizations to support business objectives and employee engagement.
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Manager HEVA BP Support SanofiBarcelona 12d Manage HEOR projects and evidence generation plans for investigational and marketed drugs to support product strategy and value proposition.
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Senior Copywriter ThermofisherBirmingham, United Kingdom 12d Senior marketing copywriter creating high-impact campaigns and coordinated tactics for diagnostics businesses, transforming complex scientific and clinical content into compelling customer-focused marketing while ensuring regulatory compliance.
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Senior Regulatory Operations Specialist MyhrabcRemote $43k–$43k12d Build, manage, and validate electronic regulatory submissions (eCTD, NeeS, XML Product Monographs, SPLs) for clients in the life sciences industry.
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Senior Manager, Regulatory Affairs BiibhrTokyo, Japan 12d Lead the development and implementation of regulatory strategy for new drug projects in Japan, serving as the regulatory representative and contact with Japanese Health Authorities.
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Product Expert – Veeva RIM Submissions, Archive, and Publishing VeevaRemote $70k–$140k12d Product expert driving customer success for Veeva Regulatory Information Management (RIM) products in Europe, focusing on Submissions, Archive, and Publishing applications.
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Medical Affairs Associate Blackmores GroupSurry Hills, New South Wales 13d Assess scientific accuracy and regulatory compliance for promotional materials, evaluate clinical evidence to substantiate health claims, and provide scientific/regulatory input for product development and market readiness.
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Multilingual Medical Information Specialist - Korean/English ProPharma GroupMelbourne, Victoria 13d Provide high-quality medical information services, handle technical product enquiries, and translate documents between English and Korean for biotech and pharmaceutical clients.
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Associate Publisher SpringernatureLondon, GB $66k–$66k13d Manage a portfolio of open access journals in the clinical medicine portfolio, driving growth, development, and operational success.
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Regulatory Publishing Manager (LATAM)↗ Syneos HealthRemoto, BR 13d Leading the creation, assembly, and publishing of electronic regulatory submissions for global health authorities.
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Sr. Principal, Medical Science Liaison - VitRet Central/Northeast AlconRemote $152k–$197k13d Present scientific and clinical information on Alcon VitRet products, gather insights to influence company strategies, and drive innovation through scientific principles for the eye care industry.
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Intern, SEAT Medical & Scientific Affairs GsknchSingapore - Rochester Park 13d Support medical-led projects and workstreams for Wellness, Oral Health, and OTC categories by generating scientific documents and supporting claims.
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サRegulatory Publishing Manager (LATAM)↗ サイネオス・ヘルスRemote 13d Lead the creation, assembly, and publishing of electronic regulatory submissions to global health authorities, managing portfolio-level interdependencies and lifecycle management.
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Associate Account Director↗ Bluprint Oncology Concepts, LLCRemote 13d Develop and deliver scientific communications solutions, manage project strategy and execution, and foster client partnerships for life sciences organizations.
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