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64 regulatory affairs specialist clinical jobs in United Kingdom

Customer Support Specialist

Zenopa 1 Review York, England

o To log customer enquiries and complaints and ensure appropriate and timely communication with customers. o Provide basic troubleshooting and advice… CV-Library.co.uk

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Associate Regulatory Writer (UK)

McCann Complete Medical 1 Review Macclesfield, England

s, regulatory responses and other supporting documents, across a variety of therapy areas. Your excellent communication and organisational skills… McCann Complete Medical

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PVG Officer

Pharma Consulting Group Hampshire

Case Processing Adverse Events Case Narrative writing Assisting with the review and development of SOPs when necessary Data Entry using relevant… Jobsite.co.uk

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Talent Acquisition Manager

Axess Ltd Richmond, London, England

AXESS seeks an experienced pharmaceutical recruitment consultant to join their expanding team and take responsibility as practice manager for a… Jobsite.co.uk

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Regulatory Affairs Specialist II (Medical Device)

Smith & Nephew 100+ Reviews United Kingdom

include the following. Other duties may be assigned. 1. Assists with the review of new products with Product Development to… Smith & Nephew

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Medical Product Labelling Specialist 6 month contract - MPLS – new

Amdipharm Mercury London, England

of product characteristics (SPCs), patient information leaflets/literature (PIL) and Clinical Expert Statements (CESs) in compliance w… Amdipharm Mercury

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Market Access Manger- London- Permanent- £70

Optimus Search Limited 4 Reviews City of London, England

- * Developing and implementing brand-specific Market Access plans and performing risk assessments. * Liaise and work closely with European and… Jobsite.co.uk

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Market Access Manger- London- Permanent- 70 – new

Optimus Search Limited 4 Reviews Yorkshire and the Humber

- Developing and implementing brand-specific Market Access plans and performing risk assessments. Liaise and work closely with European and global… Adzuna

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Senior Safety Reporting Specialist

Pharmaceutical Product Development 100+ Reviews Cambridge, East of England, England

It is advantageous that the PVG SSRS maintains knowledge and understanding of PPD's SOPs and WPDs; current global regulations and ICH/local… Pharmaceutical Product Development

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Associate, Evidence Evaluation Specialist (Medical Device)-Clinical

Smith & Nephew 100+ Reviews United Kingdom

Assist with interdepartmental collaborations, evidence assessments, and subsequent external communications. Work with marketing, PMS, regulatory… Smith & Nephew

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Evidence Evaluation Specialist (reg. guidance gov., clinical eval. reports) Medi

Smith & Nephew 100+ Reviews United Kingdom

Work with medical and scientific experts and further developing an understanding of trends within the medical and scientific… Smith & Nephew

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Sr. Scientific Evidence Specialist (evidence mng., scientific comm., publication

Smith & Nephew 100+ Reviews United Kingdom

The Scientific Evidence Specialist (SES) is responsible for providing scientific support to both internal and external customers, including advisory… Smith & Nephew

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Associate, Evidence Evaluation (Medical Device-Product Research)

Smith & Nephew 100+ Reviews United Kingdom

Assist with interdepartmental collaborations, evidence assessments, and subsequent external communications. Work with marketing, PMS, regulatory… Smith & Nephew

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Regulatory Affairs Specialist - Slough - 12 Month - £65/ hour – new

Optimus Search Limited Slough, Berkshire, South East England, England

* Working alongside the Senior Regulatory Affairs Manager, you will be involved in the preparation, maintenance and management of clinical trial… Jobsite.co.uk

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