Regulatory Medical Writer

.Regulatory Medical Writer page is loaded## Regulatory Medical Writer locations:
Stratford (2 Redman Place):
Home Based - Scotland (35 Hour Weekly Max):
Home Based - Northern Ireland (35 Hour Weekly Max):
Home Based - England (35 Hour Weekly Max):
Home Based - Wales (35 Hour Weekly Max) time type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
January 11, 2026 (8 days left to apply) job requisition :
R032497## Hyper intelligence. Curious mindsets. Accelerated progress.##
** Regulatory Medical Writer**£36,000 - £49,000 plus
*
* Reports to:

** Medical Writing Manager
** Directorate:
** Research & Innovation
*
* Contract:

** Permanent
*
* Hours:

** Full time 35 hours per week ( flexible working requests considered, minimum 32 hours per week)
*
* Location:

** Stratford, London (1-2 days a week in the office)   
** We’re happy to offer home-based contracts through our flexible working policy.
**** Visa sponsorship:
** You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is
** not
* * able to offer visa sponsorship.
** Recruitment process:
** Competency based interview followed by Medical Writing Task
** At Cancer Research UK, we exist to beat cancer.
** The Cancer Research UK Centre for Drug Development (CDD) is the world's only charity-funded drug development facility. Our pioneering research is driven purely by the goal to see scientific breakthroughs bring benefits to patients sooner. CDD is the sponsor of early phase and precision medicine clinical trials in oncology agents. Our broad portfolio rivals that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in.

As a Medical Writer you’ll be providing broad medical writing expertise for the production of clinical study reports, investigator brochures and other clinical/scientific reports for CDD’s early phase oncology trials.  As well as acting as lead author on your assigned projects and performing quality control review of documents produced by other Medical Writers, you will be fully embedded within a multidisciplinary, cross functional project team along with other CDD departments.

Collaboration is essential, as well as the ability to work strategically within an evolving environment.

Unfortunately, this role is not suitable for anyone who only has experience in medical writing for pharmacovigilance or medical devices or anyone who only has medical writing experience within science comms. You must come with strong knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results. This is a great opportunity for a current Regulatory Medical Writer looking to move into a more purpose driven environment or to gain valuable experience withing phase 1 oncology trials.

Or you could be a Medical Writing Associate ready to take that next step.
* Writing, editing, reviewing and quality control of documents for the timely production of clinical study reports and investigator brochures.
* Managing the preparation of clinical study reports by building consensus with the project teams on report requirements, responsibilities for delivery of data and production timelines, and participating in the preparation and review of summary clinical trial results and other disclosures as required.
* Managing the scheduling, preparation and updating of investigator brochure packages in use in CDD‑sponsored trials, ensuring review at least annually in line with current regulations.
* Liaising with the project team to complete project-specific tasks including review of protocols, Trial Master Files, data (including expert reports), and analytical plans.
* Proven experience in medical / medical sciences writing. This should include significant experience in regulatory medical writing or a mix of experience in regulatory medical writing plus substantial relevant experience in a related role in clinical trials, pharmacovigilance or medical writing.
* Science graduate or equivalent experience of scientific writing.
* Good knowledge of…