Medical Writing
717 open positions
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Associate Director, Regulatory Affairs MsdZAF - Gauteng - Midrand, ZA 5d 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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Advisor, MIDC AstraZenecaChina 5d 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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Signatory Lead↗ NovartisLondon, ENG, GB $68k–$126k5d Final medical signatory ensuring promotional and non-promotional materials comply with ABPI Code of Practice, regulations, and Novartis policies.
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Senior Director, Medical Affairs Edwards2 Locations $209k–$209k5d 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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Global Value Dossiers Writer - Global Health Economics team - Lisbon (hybrid/home-based)↗ IqviaOeiras, P11, PT 5d 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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サManager, FSP 360↗ サイネオス・ヘルスBuenos Aires, B, AR 5d Manager leading Functional Service Provider (FSP) partnerships to support drug development and commercialization for life sciences customers.
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Associate Content Acquisition Manager WileyBeijing, CHN, CN 5d 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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Medical Lead, Singapore & Distribution Markets and Medical Launch Lead, Asia AbbVieSingapore 5d 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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[MA] Vaccines Medical Affairs Scientist, Manager PfizerJapan - Tokyo 7d 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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Associate Medical Editor - Portuguese (Brazil) (MD/DO) AmbossSão Paulo, Estado de São Paulo 7d Physician medical editor creating and reviewing high-quality medical education content for students in Brazil.
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Senior Regulatory Operations Specialist MyhrabcRemote $43k–$43k8d Build, manage, and validate electronic regulatory submissions (eCTD, NeeS, XML Product Monographs, SPLs) for clients in the life sciences industry.
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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 8d Senior Regulatory Consultant managing dedicated regulatory portfolios for pharmaceutical sponsors, supporting global regulatory affairs and submission strategies.
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Senior Copywriter ThermofisherBirmingham, United Kingdom 8d 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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Principal Associate, Regulatory Affairs CslAPAC, AU, Victoria, Melbourne, CSL Limited Melbourne 8d Develop regulatory strategies and manage product registrations for prescription medicines in Australia and New Zealand.
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Manager HEVA BP Support SanofiBarcelona 8d Manage HEOR projects and evidence generation plans for investigational and marketed drugs to support product strategy and value proposition.
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Senior Manager, Regulatory Affairs BiibhrTokyo, Japan 8d 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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Associate Director, PDS Communications, Product Development & External Manufacturing BristolmyerssquibbPrinceton - NJ - US $157k–$157k8d 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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Product Expert – Veeva RIM Submissions, Archive, and Publishing VeevaRemote $70k–$140k8d 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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サRegulatory Publishing Manager (LATAM)↗ サイネオス・ヘルスRemote 9d 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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Senior Associate Project Manager, Medical Operations AmgenIndia - Hyderabad 9d Plans and drives execution of cross-functional projects for publications, medical content, and congress deliverables within the Scientific Communications portfolio.
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Expert Medical Systems Products Drugs FreseniusmedicalcareBengaluru, KA 9d Compiling and updating drug dossiers with a focus on clinical data, providing answers to regulatory authorities on medical/pharmacological questions, and supporting drug development projects.
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Associate Account Director↗ Bluprint Oncology Concepts, LLCRemote 9d Develop and deliver scientific communications solutions, manage project strategy and execution, and foster client partnerships for life sciences organizations.
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Intern, SEAT Medical & Scientific Affairs GsknchSingapore - Rochester Park 9d Support medical-led projects and workstreams for Wellness, Oral Health, and OTC categories by generating scientific documents and supporting claims.
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Regulatory Publishing Manager (LATAM)↗ Syneos HealthRemoto, BR 9d Leading the creation, assembly, and publishing of electronic regulatory submissions for global health authorities.
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Manager, Regulatory Affairs CMC with Viral Vector experience GileadNetherlands - Hoofddorp 9d Lead Regulatory Affairs CMC for clinical and commercial cell therapy programs, ensuring high-quality regulatory deliverables and alignment with EMA/EU requirements.
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Senior Medical Research Coordinator AbbottChina > Shanghai : 388 W. Nanjing Road, Ciros Plaza 9d Coordinate global scientific studies and manage contracts to support Abbott Core Diagnostics Medical and build scientific performance.
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Associate Publisher SpringernatureLondon, GB $66k–$66k9d Manage a portfolio of open access journals in the clinical medicine portfolio, driving growth, development, and operational success.
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