Medical Writing
734 open positions
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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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ManagerⅡ,RA TA Group, Regulatory Affairs(Oncology) AbbVieTokyo, Tokyo, jp 9d Execute regulatory affairs activities for oncology projects, ensuring timely submission of documents to PMDA/MHLW and supporting global regulatory strategy.
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Medical Affairs Associate Blackmores GroupSurry Hills, New South Wales 9d 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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Director Regulatory Affairs ANZ CSL PlasmaMelbourne, Victoria 9d Lead national regulatory operations and strategy for CSL's biotechnology products in Australia and New Zealand, serving as the primary interface with Health Authorities.
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Multilingual Medical Information Specialist - Korean/English ProPharma GroupMelbourne, Victoria 9d 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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Medical Manager Specialty Care NOLA Cluster PfizerColombia - Bogota - Suba 9d Develop and execute medical strategy for the North of Latin America (NOLA) cluster, integrating clinical evidence and stakeholder insights to guide prelaunch, launch, and lifecycle stages.
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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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Associate Director, Advertising and Promotional Compliance, US AstraZenecaUS - Boston - MA $150k–$150k9d Regulatory Affairs representative responsible for reviewing and approving regulatory content for prescription drug promotion, disease awareness, and public affairs communications.
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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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Medical Director Pulmonary SanofiCambridge, MA, US 9d Lead the development and execution of the US medical/scientific strategy for Pulmonary products, serving as the product expert for internal stakeholders and external healthcare professionals/payers.
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Sr. Principal, Medical Science Liaison - VitRet Central/Northeast AlconRemote $152k–$197k9d 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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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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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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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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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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Operational Bidding Specialist ThermofisherRemote, Mexico 9d Prepare and deliver competitive operational bids and proposals for Regulatory Affairs and Medical Writing services to support clinical research opportunities.
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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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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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Medical Education Manager Novo NordiskNew South Wales 9d Lead the development and delivery of medical education programmes to translate scientific evidence into practice for healthcare professionals treating diabetes and obesity.
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Senior CMC Regulatory Affairs Manager AbCelleraVancouver $150k–$150k9d Lead global CMC regulatory strategy and documentation for biologics programs from pre-clinical through commercialization, ensuring alignment with health authority requirements.
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Therapy Area Medical Head, Oncology (Associate Director) MsdGBR - London - London (Moorgate WeWork), GB 10d Lead an oncology therapy area team in the UK, coordinating office-based and field medical activities to deliver strategic medical plans and support the full product lifecycle.
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Senior Medical Content Writer (x/f/m) DoctolibBerlin 10d Creating and managing high-quality medical content (articles, videos, interactive content) for the Doctolib app to empower patients and healthcare professionals across Europe.
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Scientist II Medical Writing CardinalhealthPhilippines-Bonifacio Global City-Taguig 10d Creates clear, accurate, and compliant documents to communicate complex clinical and scientific data for regulatory submissions, clinical research, and scientific communications.
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JAPAC Director of Medical Excellence↗ Amgen Asia Pacific Pte. Ltd.Bugis, S00, SG 10d Strategic leadership role managing medical strategy execution, organizational agility, and talent development across the JAPAC region.
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Associate Director, Medical Affairs - Coagulation CslAmericas, US-PA, King of Prussia, CSL Behring 10d Leading the development and execution of the US Medical Affairs strategy for assigned therapeutic areas, serving as a trusted scientific partner to internal and external stakeholders.
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Associate Medical Editor - Portuguese (Brazil) (MD/DO) AmbossBrazil 10d Physician medical editor creating and reviewing high-quality medical content for international medical students, with a focus on the Brazilian market.
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Sr Director, Government Affairs↗ Gilead SciencesBerlin, BE, DE 11d Lead Gilead Germany's Government Affairs team to build influence with federal and state policymakers, shape health and pharmaceutical policy, and ensure patient access to innovative therapies.
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Federal Government Affairs Manager NeurocrineUS DC Office $120k–$120k11d Develop and execute federal legislative and policy strategies to advance patient access, pharmaceutical coverage, and reimbursement priorities.
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