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484 senior regulatory affairs associate jobs in United Kingdom

Senior Regulatory Affairs Associate

Novella Clinical 27 Reviews Scotland

of this role include: • Preparation of regulatory documentation and submissions for product approvals. • Production and review of design dossiers… Novella Clinical

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Senior Regulatory Affairs Associate - NEW ROLE! – new

Key People Limited City of London, England

- It is essential that you have a strong working knowledge of all aspects of an MRP/DCP submission. - Registrations and Post Approval submissions… Jobsite.co.uk

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Senior Associate Regulatory Affairs

C.K. Associates Limited 4 Reviews Cambridge, East of England, England

will include: - Ensuring compliance via timely submissions to regulatory agencies - Reviewing the regional component of the Global Regulatory Plan… Jobsite.co.uk

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Senior Regulatory Affairs Associate – new

Gold Group Ltd. 1 Review Buckinghamshire

This position supports the operational management of Clinical Trial Applications (CTAs) to regulatory authorities within the EAME region and is… Adzuna

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Senior Regulatory Affairs Associate

Grace James HR Glasgow, Scotland

and duties will include; •Preparation of regulatory documentation and submissions for product approvals. •Production and review of design… CV-Library.co.uk

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Senior Regulatory Affairs Associate - NEW ROLE! – new

Key People Pharmaceutical London

- It is essential that you have a strong working knowledge of all aspects of an MRP/DCP submission. - Registrations and Post Approval submissions… Glassdoor

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Senior Associate Regulatory Affairs

CK Group (Science, Clinical, IT and Engineers) Cambridge, East of England, England

will include: - Ensuring compliance via timely submissions to regulatory agencies - Reviewing the regional component of the Global Regulatory Plan… CV-Library.co.uk

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EMEA Regulatory Affairs Senior Associate / Project Manager

Novartis Pharmaceuticals 100+ Reviews Frimley, England

Interacts with global, regional and affiliate stakeholders including regulatory affairs, clinical, medical affairs, medical safety, R&D… Glassdoor

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Regulatory Affairs Senior Associate - EMEA Regulatory Affairs - Established Prod

Johnson & Johnson 100+ Reviews High Wycombe, England

At Janssen Research & Development, LLC, we are united and energized by one mission - to discover and develop innovative medicines that ease patients… Adzuna

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Regulatory Affairs Senior Manager\Associate Director - CMC

Regulatory Professionals 2 Reviews Hertfordshire

Our client is a leading global contract research organization supporting their clients from clinical & drug discovery stages, through to post… Jobsite.co.uk

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EMEA Regulatory Affairs Senior Associate / Project Manager

Frimley, England

Interacts with global, regional and affiliate stakeholders including regulatory affairs, clinical, medical affairs, medical safety, R&D… Glassdoor

EMEA Regulatory Affairs Senior Associate / Project Manager

Alcon 100+ Reviews Frimley, England

Interacts with global, regional and affiliate stakeholders including regulatory affairs, clinical, medical affairs, medical safety, R&D… Glassdoor

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EMEA Regulatory Affairs Senior Associate / Project Manager

Novartis 100+ Reviews Frimley, England

Interacts with global, regional and affiliate stakeholders including regulatory affairs, clinical, medical affairs, medical safety, R&D… Glassdoor

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  • Salaries

EMEA Regulatory Affairs Senior Associate / Project Manager

Novartis UK 3 Reviews Frimley, England

Interacts with global, regional and affiliate stakeholders including regulatory affairs, clinical, medical affairs, medical safety, R&D… Glassdoor

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Senior Regulatory Affairs Associate

Johnson & Johnson 100+ Reviews High Wycombe, England

Janssen At Janssen, we are dedicated to addressing and solving some of the most important unmet medical needs of our time in oncology, immunology… Adzuna

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Regulatory Affairs Programme Manager \ Senior Manager \ Associate

Regulatory Professionals 2 Reviews East of England

will include: Line management of the post approval project team - approx 5 staff Day to day management and monitoring of the work programme Monthly… Jobsite.co.uk

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UK/Europe - Sr Regulatory Affairs Specialist - Per

Novella Clinical United Kingdom

· At least 5 years’ experience in medical devices regulatory affairs, within industry or a CRO environment. · Extensive knowledge of medical… Novella Clinical

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