2,352

Clinical Trial jobs in United Kingdom

Lead Regulatory Writer & Submissions Strategy

Certara

United Kingdom
On-site
GBP 65,000 - 80,000
21 days ago
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Assistant Technical Officer Pharmacy Aseptic Services | The Royal Wolverhampton NHS Trust

Royal Wolverhampton NHS Trust

Wolverhampton
On-site
GBP 40,000 - 60,000
21 days ago

Theatre Practitioner - Orthopaedic Theatre

University Hospitals of Derby and Burton NHS Foundation Trust

East Midlands
On-site
GBP 25,000 - 33,000
21 days ago

Staff Nurse (BAND 5) - Medical Day Unit | The Royal Marsden NHS Foundation Trust

The Royal Marsden NHS Foundation Trust

Greater London
On-site
GBP 30,000 - 38,000
21 days ago

Higher Level Pharmacist - Aseptic and Cancer Services | The Royal Wolverhampton NHS Trust

Royal Wolverhampton NHS Trust

Wolverhampton
On-site
GBP 35,000 - 45,000
21 days ago
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Part-Time Clinical Research Nurse - Mental Health

NHS

Peterborough
On-site
GBP 38,000 - 47,000
22 days ago

Senior Vice President Business Development

EPM Scientific

Liverpool
Remote
GBP 150,000 - 200,000
22 days ago

Account Director (Medical Communications)

Ogilvy UK

Greater London
Hybrid
GBP 80,000 - 100,000
22 days ago
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Founding Engineer

Delfa AI

Greater London
On-site
GBP 100,000 - 120,000
24 days ago

BI Report Developer

Triumph Research Intelligence Limited

Cambridge
Remote
GBP 50,000 - 58,000
24 days ago

Senior Global PV Case Processing Lead & SME

CSL Plasma

Maidenhead
On-site
GBP 70,000 - 90,000
24 days ago

Senior In Vivo Imaging Scientist

Taylorollinson

Macclesfield
On-site
GBP 43,000 - 49,000
24 days ago

Senior Technician, Aseptic Services | The Royal Marsden NHS Foundation Trust

THE ROYAL MARSDEN

Greater London
On-site
GBP 40,000 - 60,000
24 days ago

Senior Medical / Scientific Director, SERM

1054 GlaxoSmithKline Services Unlimited

Greater London
On-site
GBP 80,000 - 100,000
24 days ago

Head of AI Transformation

AstraZeneca

Hull and East Yorkshire
On-site
GBP 70,000 - 90,000
24 days ago

Clinical Research Practitioner — Patient‑Centered Trials

NHS

Camberley
On-site
GBP 28,000 - 32,000
24 days ago

Paediatric Research Nurse — Clinical Trials & Training

King's College Hospital

Orpington
On-site
GBP 30,000 - 45,000
24 days ago

Associate Research Practitioner

NHS

Camberley
On-site
GBP 28,000 - 32,000
24 days ago

Lead Pharmacist – Aseptic & Technical Services

Sandwell and West Birmingham Hospitals NHS Trust

West Bromwich
On-site
GBP 45,000 - 65,000
24 days ago

Principal Pharmacist - Technical Services

Sandwell and West Birmingham Hospitals NHS Trust

West Bromwich
On-site
GBP 45,000 - 65,000
24 days ago

Locum Consultant Respiratory Physician PVDU

NHS

Cambridge
On-site
GBP 80,000 - 100,000
24 days ago

Research Nurse

University College London Hospitals NHS Foundation Trust

City of Westminster
On-site
GBP 31,000 - 40,000
24 days ago

Building Management System Technician

NHS

Burton upon Trent
On-site
GBP 31,000 - 35,000
24 days ago

Staff Nurse (BAND 5) - Olayan day care

The Royal Marsden NHS Foundation Trust

Sutton
On-site
GBP 25,000 - 32,000
24 days ago

Executive Medical Director/SERM Head - Oncology

GlaxoSmithKline

Greater London
On-site
GBP 204,000 - 341,000
24 days ago

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Lead Regulatory Writer & Submissions Strategy
Certara
United Kingdom
On-site
GBP 65,000 - 80,000
Full time
21 days ago

Job summary

A leading drug development consulting firm in the United Kingdom is looking for an experienced Associate Principal Regulatory Writer. The role involves leading project teams in preparing high-quality regulatory documents, mentoring junior staff, and managing project budgets. Candidates should have a Bachelor's degree, a minimum of 8 years of regulatory writing experience, and strong proficiency in Microsoft Word. Join us to contribute to advancing critical therapies for patients.

Qualifications

  • 8+ years of regulatory writing experience or equivalent experience.
  • Understand regulatory authority guidelines and requirements.
  • Experience in the development of submission-level documents.

Responsibilities

  • Prepare high quality documentation for regulatory submissions.
  • Lead development of strategies for organizing regulatory documents.
  • Manage budget for low complexity projects.

Skills

Intermediate proficiency with Microsoft Word
Strong understanding of the document creation process
Ability to synthesize data across multiple sources
Expertise in quality document preparation
Ability to own submission-level sections
Understanding of communication best practices

Education

Bachelor’s degree; MS or PhD preferred
Job description
A leading drug development consulting firm in the United Kingdom is looking for an experienced Associate Principal Regulatory Writer. The role involves leading project teams in preparing high-quality regulatory documents, mentoring junior staff, and managing project budgets. Candidates should have a Bachelor's degree, a minimum of 8 years of regulatory writing experience, and strong proficiency in Microsoft Word. Join us to contribute to advancing critical therapies for patients.

* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.