7 Regulatory Affairs Manager Pharmaceutical Jobs in Greater London
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Regulatory Affairs Manager, Global Regulatory Affairs Pharmaceuticals, EU Elanco - Hook This role contributes to the regional registration activities for new and existing products by planning, coordinating, and delivering registration documentation to the regulatory agencies for assigned... 63000 USD 9 days ago
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Regulatory Affairs Senior Manager Park Street People - Uxbridge, London, United Kingdom Strong communication and stakeholder management experience, you will be able to demonstrate working in project teams, where you have guided/advised on the implementation of your strategy/regulatory plan... £46 - £48/hour Yesterday
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Regulatory Affairs Senior Manager Park Street People - Uxbridge, United Kingdom Strong communication and stakeholder management experience, you will be able to demonstrate working in project teams, where you have guided/advised on the implementation of your strategy/regulatory plan... 13 days ago
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Regulatory Affairs CMC Manager Cpl Life Sciences - Uxbridge, United Kingdom Manages strategy and execution for all regulatory CMC submissions (e.g. late-stage clinical trials, variations, extensions and marketing applications) for products within the portfolio in compliance with... 16 days ago
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CMC Regulatory Affairs Manager Park Street People - Uxbridge, London, United Kingdom This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science. Liaise... £40 - £43/hour 28 days ago
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Head of Regulatory Affairs (Emerging Markets/ROW) Walker Cole International - London, United Kingdom Regulatory Affairs | RA | Senior Manager | Manager | EU | European Union | MHRA | EMA | European Medicines Agency | Post-approval | New Product Introduction | Product Launch | MAA | Marketing Authorisation... 3 days ago
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Regulatory Strategy and Submissions Manager greater london, england, United Kingdom As a Regulatory Affairs Professional, you will assume a crucial role in providing leadership and expertise in all regulatory and submission-related aspects of clinical trials. You will serve as the main... 28 days ago
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