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152 Clinical Regulatory Documents Associate Jobs in United Kingdom

Administrator (Document Associate) – new

Phlexglobal 2 Reviews Amersham, England

We are looking for proactive individuals to join our fast paced, busy team. As a Document Associate you will be focussing on the operational… Reed.co.uk

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Associate Director, Regulatory Affairs, CMC – new

Kelly Services Cambridge, East of England, England

- Responsible for the submission of CMC regulatory documents to support clinical trials, original NDAs/MAAs, variations and license renewals to… Reed.co.uk

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Medical Advisor

Real Life Sciences Nottinghamshire

medical and clinical data, and the associated regulatory documentation PharmiWeb

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Senior Medical Writer opportunity with a specialist CRO

RBW Consulting Solutions Ltd South East England

worldwide. As a Senior Medical Writer you will: Write clinical documents associated with… Adzuna

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Senior Regulatory Affairs Associate

Barrington James Clinical Glasgow, Scotland

and duties will include: • Preparation of regulatory documentation and submissions for product approvals • Production and review of design… PharmiWeb

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Medical Writer II

PAREXEL 100+ Reviews Greater London

• Serve as the Medical Writing representative on assigned project teams, providing proactive support to Project Leadership for planning efficient… Glassdoor

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Clinical Trial Associate

SRG 2 Reviews Cheshire

As Clinical Trial Associate the main focus will be to support the Clinical Trial Team acting as the point of contact for TMF, study start up, from… CV-Library.co.uk

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Associate Director, Regulatory Affairs, CMC – new

Kelly Scientific UK 30 Reviews Cambridge, East of England, England

- Responsible for the submission of CMC regulatory documents to support clinical trials, original NDAs/MAAs, variations and license renewals to… Glassdoor

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Clinical Research Consultant

Gold Group Ltd. 1 Review United Kingdom

*Develop and promote the business, *Assisting Client in taking their products to the clinic; *Ensuring that study deliverables are achieved in a… TotalJobs.co.uk

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Senior Regulatory Affairs Associate, Oncology – new

Kelly Services Cambridge, East of England, England

•This position will report to the Director/Associate Director of the Oncology and Anti-Inflammatory group in International Regulatory Affairs and… Reed.co.uk

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Clinical Research Consultant

Gold Group 1 Review Cambridgeshire

*Develop and promote the business, *Assisting Client in taking their products to the clinic; *Ensuring that study deliverables are achieved in a… CV-Library.co.uk

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Clinical QA Officer, £s neg.

team 2000 Cambridge, East of England, England

An exciting opportunity has arisen with our client for a Clinical QA Officer to provide administrative support for the CQA team, in support of the… Reed.co.uk

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REGULATORY AFFAIRS, ASSOCIATE MANAGER MD&D - PERM – new

Novella Clinical Resourcing Bedfordshire

This role will provide strategic regulatory guidance and information to projects and will acquire pertinent regulatory information from agencies and… PharmiWeb

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Senior Regulatory Affairs Associate

inVentiv Health Clinical 23 Reviews London, England

Prepare and submit to clients and/or health authorities electronic regulatory submissions Review and/or supervise the review of regulatory… Adzuna

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UK-Study Start Up & Document Control Manager-Perm

Novella Clinical 25 Reviews North West England

This role is responsible for the quality and regulatory compliance of the Principal Investigator credentialing, essential documents and investigator… Novella Clinical

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Administrator (Document Quality Associate)

Phlexglobal Chesham, England

This is an exciting time to join Phlexglobal, an expanding specialist provider of technology enabled document management solutions to the global… Reed.co.uk

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