Medical Writing
1,301 open positions
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Senior Manager Regulatory Affairs US Advertising and Promotion AbbVieFlorham Park, NJ, us 1mo Senior Manager leading Regulatory Affairs for US Advertising and Promotion, ensuring compliance with FDA and other regulations for pharmaceutical products.
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Regulatory Affairs – CMC Consultant ClinChoiceUnited States - NJ 1mo Regulatory CMC expert supporting pharmaceutical and self-care product development, lifecycle management, and global regulatory submissions.
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Senior Director, Intl Regulatory Affairs Geo-Expansion VrtxPaddington, United Kingdom 1mo Senior Director leading global regulatory strategy for Vertex's international markets (EU, UK, CH, ROW) across emerging disease areas and registered medicines.
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PR-Berater:in Healthcare & Pharma (m/w/d) – Köln / Hybrid Signum Brands GmbHKöln, NORDRHEIN_WESTFALEN 1mo PR consultant for healthcare and pharma clients, developing communication strategies, managing projects, and creating scientific content.
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Redakteur*in / Medical Writer (m/w/d), Stuttgart Thieme Group / Georg Thieme Verlag KGRemote 1mo Develop medically strong, understandable, and cross-channel effective content for healthcare solutions, including newsletters, CME units, and patient care modules.
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Associate Director, WW Medical Learning, Neuro BmsPrinceton - NJ - US 1mo Define the multi-year scientific learning strategy for BMS Neurology across WW/International Markets to empower Field Medical (FM) and Home Office Medical (HOM) teams.
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Global Regulatory Affairs Director AstraZenecaCambridge, Massachusetts, United States of America $186k–$279k1mo Provide strategic and operational regulatory leadership for the development, commercialization, and life cycle management of assigned pharmaceutical products.
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Senior Associate, Regulatory Operations Publicis Groupe Holdings B.VPhiladelphia, Pennsylvania $54k1mo Project-level lead responsible for preparing promotional material submission packages for pharmaceutical clients' Medical, Legal, and Regulatory (MLR) review.
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Medical Director - Critical Care CeribellRemote $300k1mo Lead medical strategy, drive peer-to-peer engagement with sales teams, and support evidence generation for a point-of-care EEG platform in critical care.
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21GRAMS- VP, Medical Strategy Director RealchemistryRemote $180k1mo Senior strategic leader transforming complex clinical science into actionable medical strategy and compelling narratives for pharmaceutical and biotech brands.
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Group Copy Supervisor (HCP & DTC Pharma Experience Required) EversanaChicago, IL, us 1mo Lead concept and copy development for pharmaceutical marketing projects, serving as a direct liaison between creative and senior account teams to deliver work meeting strategic and business expectations.
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Scientific Projektmanager Kijimea (synformulas Gmbh)Gräfelfing/Munich 1mo 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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Associate Solution and Delivery Lead, Healthcare & Pharma IqviaBasel, Switzerland 1mo Strategic, scientific, and delivery leader for Real World Evidence (RWE) solutions, shaping client strategy and driving revenue growth for healthcare clients.
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Senior Director, Medical Affairs Edwards2 Locations $209k–$296k1mo Lead the Medical Affairs strategy for the Transcatheter Mitral and Tricuspid Therapies (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 1mo 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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(Senior) Global Medical Director (m/f/d) Migraine↗ Merz TherapeuticsFrankfurt, Hesse, Germany 1mo Provide strategic medical leadership for the migraine pipeline product and shape global Medical Affairs strategy throughout the product lifecycle.
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Korean to English Medical Linguist The Language Doctors, Inc.Sydney, New South Wales 1mo Translate Korean medical documents (patient records, medical reports) into English with accurate terminology and style consistency.
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Senior Specialist Regulatory Operations (Electronic Submissions)↗ ViatrisLisboa, Lisbon, Portugal 1mo Publish, transmit, and archive Marketing (MA) Applications and maintenance submissions in eCTD or non-eCTD formats for new and existing products, ensuring quality control and compliance with agency requirements.
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[MA] Vaccines Medical Affairs Scientist, Manager PfizerJapan - Tokyo 1mo 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 1mo 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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Senior Manager, Regulatory Affairs BiibhrTokyo, Japan 1mo 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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Medical Advisor, Neurology↗ Alexion Pharmaceuticals, Inc.Munich, Bavaria, Germany 1mo Develops and maintains scientific and medical expertise in neurological indications, supports global strategy, and acts as an external contact for medical-scientific concerns.
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Senior Regulatory Operations Specialist MyhrabcRemote CA$43k1mo Build, manage, and validate electronic regulatory submissions (eCTD, NeeS, XML Product Monographs, SPLs) for clients in the life sciences industry.
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Product Expert – Veeva RIM Submissions, Archive, and Publishing VeevaRemote €70k–€140k1mo 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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Vice President, MS - Ogilvy Health, Medical Education OgilvyOgilvy Health Parsippany 1mo Lead and oversee the development and execution of strategic medical education programs for pharmaceutical and biotech clients.
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Medical Affairs Associate Blackmores GroupSurry Hills, New South Wales 1mo 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 1mo 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 1mo 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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Expert Medical Systems Products Drugs FreseniusmedicalcareBengaluru, KA 1mo Compiling and updating drug dossiers with a focus on the clinical part, providing answers to authorities on registration-related medical/pharmacological questions, and supporting drug development projects.
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Sr. Principal, Medical Science Liaison - VitRet Central/Northeast AlconRemote $152k–$197k1mo 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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Medical Director Pulmonary SanofiCambridge, MA, US 1mo Lead the development and execution of the US medical/scientific strategy for Pulmonary products, serving as the product expert and strategic partner to Clinical, Commercial, Regulatory, and Market Access teams.
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Manager, Regulatory Affairs CMC with Viral Vector experience GileadNetherlands - Hoofddorp 1mo 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 Education Manager Novo NordiskNew South Wales 1mo 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 CA$150k1mo 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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