Cancer Research UKHiring

Principal Regulatory Medical Writer

  • GBP 50,000 to 58,000 per year
  • Remote, United Kingdom
  • Full-time
  • Lead
  • Posted 5 days ago
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In one line

Principal Regulatory Medical Writer is a lead full-time remote role in the United Kingdom at a charity-funded drug development organisation.

About the role

Clinical study reports, investigator brochures and similar documents must be accurate and filed on time for trials the group sponsors. The post sits in a writing team that supports a broad portfolio of antibodies, cell therapies, vaccines and small molecules.

At a glance

Pay
GBP 50,000 to 58,000 per year
Remote scope
Remote, United Kingdom
Seniority
Lead
Employment
Full-time
Skills
Medical Writing, Clinical Study Reports, Quality Control, SOPs
Posted
24 Oct 2026
Last checked
28 Oct 2026

What you will do

  • Write, edit, review and quality check clinical study reports and investigator brochures to regulatory deadlines
  • Track report preparation and updates, compile compliance metrics and keep document templates, SOPs and guidance current
  • Train new and junior medical writers and act as a subject matter expert for writing practice
  • Deputise for the writing manager and represent the group in cross-functional working groups
  • Review and improve document processes so output stays consistent across programmes

What they look for

  • Expert medical writing skills in a regulatory or clinical development setting
  • Experience preparing clinical study reports and investigator brochures
  • Confidence advising colleagues and mentoring less experienced writers

Benefits

  • £50,000 to £58,000 salary plus benefits
  • Flexible working, with home-based contracts available on request

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Questions about this job

Is this a remote job, and where can I work from?

The posting lists it as remote for people in the United Kingdom.

What does this job pay?

The posting states GBP 50,000 to 58,000 per year.

What experience is needed?

It is a lead role. The posting asks for: expert medical writing skills in a regulatory or clinical development setting; experience preparing clinical study reports and investigator brochures; confidence advising colleagues and mentoring less experienced writers. Skills it names include Medical Writing, Clinical Study Reports, Quality Control, SOPs.

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