Medical Writing Manager

Cancer Research UK (CRUK); Gildersome; Hybrid; GBP 70,000 - 77,000; Full time

Job summary

Cancer Research UK in London is seeking a Medical Writing Manager to lead the medical writing function within the Centre for Drug Development. You will deliver regulatory compliant Clinical Study Reports, Investigator Brochures, and other reports, driving innovation and risk-based approaches.

This role reports to the Head of Biometrics and Medical Writing, offers a permanent, full-time scheme with 35 hours per week, hybrid working (1–2 days in office) and occasional travel to Stratford.

Qualifications

• Extensive experience in Medical Writing and regulatory reports.
• Proven ability to lead cross-functional teams.
• Strong regulatory knowledge for IBs, CSRs and trial reports.
• Excellent written and verbal communication with stakeholders.
• Fluent English with keen attention to detail.

Responsibilities

• Lead the medical writing function to deliver high-quality reports within regulatory timelines.
• Provide specialist writing support across the portfolio and trials.
• Line manage the Medical Writing team and ensure appropriate resourcing.
• Produce/QA Clinical Study Reports, Investigator Brochures and summaries.
• Oversee IB Packages and updates per trial regulations.
• Review third-party IBs and assess need for supplements.
• Oversee results reporting across trials including lay summaries.
• Drive continuous improvement of processes and systems.

Skills

Medical writing

Project leadership

Regulatory knowledge

Stakeholder engagement

English proficiency

Education

Bachelor's degree in life sciences

Tools

AI drafting tools

Job description

4,000 professionals, 0 days wasted, 1 incredible purpose. Together we are beating cancer.

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).

Travel & Expenses

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

Eligibility

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.

Company overview

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.

What will you 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.

What skills are we looking for?

• Educated to a minimum of Bachelor’s degree level in a life science or medical discipline or related field.
• Extensive experience in Medical Writing, writing regulatory reports and clinical/scientific documents in a medical/pharmaceutical field.
• Thorough knowledge of regulatory requirements for relevant clinical trial documents, including IBs, CSRs and clinical trial summary results.
• Strong interpersonal skills and able to build good working relationships with key functions in CDD to ensure timely delivery of data and documents. Able to build good relationships with stakeholders external to CDD.
• Excellent written and verbal English, proofreading skills and attention to detail.
• Proven experience in training, mentoring and/or line management in the field of Medical Writing.

Desirable

• Higher degree (Masters or PhD).
• Experience in early phase clinical development.
• Oncology experience.
• Line management experience.
• Use of AI to generate document drafts.

Values

Our organisation values are designed to guide all that we do.

Bold: Act with ambition, courage and determination

Credible: Act with rigour and professionalism

Human: Act to have a positive impact on people

Together: Act inclusively and collaboratively

We’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.

What will I gain?

We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals.

You can explore our benefits by visiting our careers web page.

Equality, Diversity and Inclusion

Our vision is to create a charity where everyone feels like they belong, benefits from and participates in, the work we do. We actively encourage applications from people of all backgrounds and cultures, in particular those from ethnic minority backgrounds who are currently under-represented.

We want to see every candidate performing at their best throughout the job application process, interview process and whilst at work. We therefore ask you to inform us of any concerns you have or any adjustments you might need to enable this to happen.

Unfortunately, we are unable to recruit anyone below the age of 18, so that we can protect young people from health & safety and safeguarding risks.