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6,337

Clinical Research Associate jobs in United Kingdom

Regulatory Documentation Scientist

Proclinical Staffing

England
Hybrid
GBP 40,000 - 60,000
15 days ago
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Junior Research Scientist

Story Terrace Inc.

Greater London
On-site
GBP 45,000 - 75,000
15 days ago

Regulatory Documentation Scientist

Proclinical

England
On-site
GBP 50,000 - 70,000
15 days ago

Regulatory Documentation Scientist (Remote/Hybrid)

Proclinical Group

England
Hybrid
GBP 50,000 - 70,000
15 days ago

Data Scientist

Halliburton

Abingdon
On-site
GBP 50,000 - 70,000
15 days ago
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Band 6 Haematology Biomedical Scientist - Dundee City - Sanctuary Personal

Sanctuary Personnel Ltd

Dundee
On-site
GBP 60,000 - 80,000
15 days ago

Senior RF Data Scientist & ML Research Engineer (Cambridge)

Adria Solutions Ltd.

Saffron Walden
Hybrid
GBP 60,000 - 80,000
15 days ago

Senior RF Data Scientist / Research Engineer

Adria Solutions Ltd.

Saffron Walden
Hybrid
GBP 60,000 - 80,000
15 days ago
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Permanent Data Scientist - Enhanced DV Clearance | London

Searchability

Greater London
On-site
GBP 80,000 - 95,000
15 days ago

Data Scientist - eDV Cleared

Searchability

Greater London
On-site
GBP 80,000 - 95,000
15 days ago

Senior Data Scientist

Solirius Consulting

Greater London
On-site
GBP 60,000 - 80,000
15 days ago

Senior AI Data Scientist

Halliburton Energy Services

Abingdon
On-site
GBP 100,000 - 125,000
15 days ago

Senior RF Data Scientist — ML & Prototyping for UAVs

Adria Solutions Ltd

Cambridgeshire and Peterborough
Hybrid
GBP 55,000 - 75,000
15 days ago

Senior AI Data Scientist - Build Impactful ML Solutions

Solirius Consulting

Greater London
On-site
GBP 60,000 - 80,000
15 days ago

Senior RF Data Scientist / Research Engineer

Adria Solutions Ltd

Cambridgeshire and Peterborough
Hybrid
GBP 55,000 - 75,000
15 days ago

Senior AI Data Scientist — Subsurface Geospatial

Halliburton Energy Services

Abingdon
On-site
GBP 100,000 - 125,000
15 days ago

Senior RF AI/ML Data Scientist — DSP & SDR Onsite

Ecm Selection

Cambridge
On-site
GBP 50,000 - 80,000
15 days ago

Senior Data Scientist Research Engineer

Ecm Selection

Cambridge
On-site
GBP 50,000 - 80,000
15 days ago

Senior GenAI Data Scientist

Amazon

Greater London
On-site
GBP 70,000 - 90,000
15 days ago

Senior Data Scientist, Generative AI Innovation Center, AWS Generative AI Innovation Center

Amazon

Greater London
On-site
GBP 70,000 - 90,000
15 days ago

Senior Data Scientist, Generative AI Innovation Center, AWS Generative AI Innovation Center

Amazon

Greater London
On-site
GBP 70,000 - 90,000
15 days ago

Senior GenAI Data Scientist, AI Solutions

Amazon

Greater London
On-site
GBP 70,000 - 90,000
15 days ago

Lead Formulation Scientist & Team Leader (Pharma R&D)

Eurofins UK PSS

Sittingbourne
On-site
GBP 40,000 - 50,000
15 days ago

Formulation Group Lead Scientist

Eurofins UK PSS

Sittingbourne
On-site
GBP 40,000 - 50,000
15 days ago

Associate Research Practitioner | Frimley Health NHS Foundation Trust

Frimley Health NHS Foundation Trust

Camberley
On-site
GBP 60,000 - 80,000
30 days ago

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Regulatory Documentation Scientist
Proclinical Staffing
England
Hybrid
GBP 40,000 - 60,000
Full time
15 days ago

Job summary

A leading regulatory consulting firm in the United Kingdom is seeking a Regulatory Documentation Scientist to ensure high-quality, compliant documentation for regulatory submissions. The role involves collaborating with cross-functional teams to prepare and submit nonclinical regulatory documents. Key qualifications include a life sciences degree and experience in scientific writing. This position offers flexibility with remote or hybrid work options, promoting a balance between productivity and collaboration.

Qualifications

  • Experience in scientific writing and editing within a nonclinical regulatory domain.
  • Proficiency in writing and editing software, with interest in new tools.
  • Strong collaboration and communication skills with diverse stakeholders.

Responsibilities

  • Manage the preparation, review, and submission of nonclinical documents.
  • Collaborate with regulatory and scientific teams for accurate dossiers.
  • Draft regulatory submission documents and research-related materials.

Skills

Scientific writing
Editing
Collaboration
Communication
Problem-solving

Education

University degree in life science

Tools

Writing and editing software
Job description

Crafting compliant, high-impact regulatory documents that drive global drug development forward.

Proclinical is seeking a Regulatory Documentation Scientist to support the preparation and submission of nonclinical regulatory documents. This role focuses on ensuring high-quality, compliant documentation for regulatory submissions, including INDs, CTAs, NDAs, MAAs, and BLAs. You will collaborate with cross‑functional teams to deliver accurate and impactful scientific content.

This position offers flexibility with remote or hybrid work options, empowering you to balance productivity and collaboration.

Responsibilities
  • Manage the preparation, review, and submission of nonclinical summary documents for early development and marketing applications.
  • Collaborate with regulatory and scientific teams to ensure comprehensive and accurate nonclinical dossiers are submitted to health authorities.
  • Work closely with Nonclinical Project Leaders and Scientists to draft regulatory submission documents, study reports, and other research-related materials.
  • Develop and maintain processes, tools, and guidelines to ensure high-quality document production.
  • Represent the nonclinical team in global regulatory initiatives and projects focused on process and technology improvements.
Key Skills and Requirements
  • A university degree in a life science discipline.
  • Experience in scientific writing and editing within a nonclinical regulatory domain.
  • Proficiency in writing and editing software, with an interest in exploring new tools and technologies.
  • Strong collaboration and communication skills, with the ability to build trust and work effectively with diverse stakeholders.
  • A commitment to producing high-quality, customer-focused documentation.
  • Proactive problem-solving skills and a sense of ownership over your work.

If you are having difficulty in applying or if you have any questions, please contact Peter Duvall at p.duvall@proclinical.com.

Apply Now

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

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* 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.

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