48 Drug Regulatory Affairs Jobs - page 2
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Senior Regulatory Affairs Consultant (Label Strategist) Parexel - United Kingdom Solid aptitude for use of IT systems; Regulatory Information Management System (RIMS), electronic document management system (EDMS). Ability to manage the review and approval of labeling in a document... Competitive 6 days ago
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Regulatory Affairs Manager ICON Strategic Solutions - United Kingdom, Homeworking Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs... Competitive 7 days ago
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Principal Consultant (Clinical) Morgan Prestwich - Life Science & Healthcare Executive Search - England Morgan Prestwich Executive Search is committed to providing a diverse range of talent to our clients. We do not discriminate based on race, religion or sex throughout our screening and matching process... 2 days ago
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Labelling, Artwork & Translations – Regulatory Manager Cambridge, England, United Kingdom You will be responsible for contributing to the definition, development, and implementation of process improvements and initiatives to meet the evolving needs of the LAT group. You will represent LAT on... 10 days ago
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Manager, Regulatory Affairs-hybrid role abingdon, england, United Kingdom Preparation of regulatory submissions including: INDs, CTAs, GMOs, IDEs, amendments, annual reports, meeting briefing documents, responses to regulatory agency information requests, marketing authorization... 14 days ago
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Principal Clinical Consultant, Career Growth, UK - Remote NonStop Consulting - England, England Broad experience in a lot of different clinical documentation( also RA related) like Clinical and Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing... £ 120000.00 - £ 140000.00 Per Yr More than 30 days ago
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Associate Director, Quality Control Oxford, England, United Kingdom Gain a comprehensive understanding of Moderna's Quality Control processes and standards, specifically focusing on the nuances of commercial testing functions for mRNA products. This includes familiarization... 13 days ago
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US Medical Affairs Lead, Specialty New Medicines GlaxoSmithKline - Collegeville, PA 19426, USA Develops the US strategy and operational plan for Specialty assets in the pipeline laying the initial foundation for future US Medical Affairs launches; Performs advanced scenario-planning and preliminary... 4 days ago
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Global Medical Senior Director CNP Ascendis Pharma - Hellerup, Denmark Works closely with Compliance, Legal and Regulatory to ensure that all Global Medical Affairs activities and services are fully compliant with Ascendis SOPs as well as global regulatory and compliance... 12 days ago
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Senior Scientific Claims Manager (1 Year Contract) - London - £50-60,000 Senior Scientific Clai[...] London, England, United Kingdom You will liaise proactively with the UK legal team , international claims and regulatory groups. Using your strong interpersonal skills you will build strong and collaborative relationships with both internal... 15 days ago
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