Medical Writing Manager

Salary: £70,000 - £77,000 plus benefits

Reports to: Head of Biometrics and Medical Writing

Department: Research & Innovation

Contract: Permanent

Hours: Full-time, 35 hours per week (requests for compressed hours or flexible working would be considered).

Location: Stratford, London (high flex 1-2 days per week in the office, or Homebased on request).

We’re happy to offer home-based contracts through our flexible working policy. While this role does involve occasional travel to our Stratford Office — typically 4 to 6 times a year, please note that travel expenses are not covered. We aim to keep travel minimal and purposeful, ensuring it adds real value to your work and team collaboration.

Closing date: Sunday 13th September at 23:55pm

Interview process: Competency-based interview process.

Interview dates: W/C 21st September

Please note: You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is not able to offer visa sponsorship.

About the Role

At Cancer Research UK, we exist to beat cancer.

We have an exciting new opportunity for a Medical Writing Manager to lead and develop the medical writing function in the Centre for Drug Development (CDD). In this role you will provide broad medical writing expertise and ensure the timely production of regulatory compliant Clinical Study Reports, Investigator Brochures, and other clinical/scientific reports. In addition, you will drive innovation within the team, looking for opportunities to adopt new solutions and risk-based approaches to improve efficiencies.

About the Team

The Cancer Research UK Centre for Drug Development (CDD) is the world's only charity-funded drug development organisation. 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.

What You Will Be Doing

• Manage the medical writing function in CDD, to achieve best practice and deliver agreed CDD documents to a high quality within applicable regulatory guidelines and timeframes.
• Provide specialist support to project teams, including advice to support strategies for medical writing deliverables across the portfolio, developing processes for complex, high-priority and international clinical trials, and providing input into development and review of other key documents such as protocols, statistical analysis plans or reporting analysis plans and publications.
• Line manage Medical Writing team members to ensure continued development, performance management and appropriate resourcing across all CDD trials according to individual team members’ expertise and professional development.
• Provide specialist medical writing skills within the CDD, including writing, editing, reviewing and quality control (QC), to ensure production of Clinical Study Reports, Investigator Brochures (IBs) and summary results.
• Maintain oversight of all IB Packages in use in CDD-sponsored trials, ensuring timely generation to meet agreed goals and document updates in line with current clinical trial regulations.
• Work with Project Teams to review third-party IBs and assess the need for CRUK IB supplements.
• Maintain oversight of all results reporting across CDD-sponsored trials, including CSRs, CSR addenda, summary results for disclosure on public trial registries and lay summaries.
• Drive the continuous review of Medical Writing processes and external systems that support Medical Writing (e.g. project management, document management, proofreading, Artificial Intelligence [AI]) and ensure regulatory document templates, Medical Writing SOPs and Guidance Documents are produced and maintained to ensure consistency in format and best practice in accordance with appropriate regulatory requirements.
• Select, assess and oversee consultant resource responsible for medical writing tasks to ensure quality and timeliness of outsourced activities.