Medical Writing Manager

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

Benefits offered by this job

Home-based contracts

Flexible working policy

Occasional travel

Job summary

Cancer Research UK in Stratford, London, is seeking a Medical Writing Manager to lead and develop the medical writing function within the Centre for Drug Development. The role ensures timely production of regulatory reports such as Clinical Study Reports and Investigator Brochures, while driving process innovation and risk-based approaches to improve efficiency.

The role reports to the Head of Biometrics and Medical Writing, with responsibility for line managing the Medical Writing team and

Qualifications

• Educated to a bachelor’s degree in life sciences or related field.
• Extensive experience in Medical Writing and regulatory documents.
• Knowledge of regulatory requirements for IBs, CSRs and trial summaries.

Responsibilities

• Lead the medical writing function within the Centre for Drug Development and ensure timely delivery of regulatory documents.
• Provide specialist support to project teams on medical writing strategies for trials and publications.
• Line manage Medical Writing staff and coordinate resourcing across trials.
• Oversee creation and QC of Clinical Study Reports, Investigator Brochures and summaries.
• Review third-party IBs and assess need for supplements.
• Maintain SOPs, templates and guidance documents for consistency and compliance.
• Oversee outsourced medical writing tasks and vendor relationships.

Skills

Medical Writing

Regulatory documents

Project management

Line management

Stakeholder management

English proficiency

Education

Bachelor’s degree in life sciences

Tools

AI document drafting

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). 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.

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 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.

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?

Wecreate a working environment that supports your wellbeing andprovide agenerous benefits package, a wide range of career and personal development opportunities and high-quality tools. Ourpolicies 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 benefitsby visitingour careers web page.

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.