Regulatory Medical Writer Job Vacancy at Cancer Research UK

Hyper Intelligence. Curious Mindsets. Accelerated Progress.

Role: Regulatory Medical Writer
Salary: £36,000 – £44,000 plus benefits
Reporting to: Medical Writing Manager
Department: Research & Innovation
Contract Type: Permanent
Working Hours: Full-time, 35 hours per week (flexible working arrangements considered, with a minimum of 32 hours per week)
Location: Home-based or Stratford, London (1-2 days per week in the office)
Application Deadline: 08 December 2024, 23:55

Please note: This position may close sooner if a high volume of applications is received or once an ideal candidate is identified. We recommend applying early to avoid missing out. If you have any concerns about the recruitment process or require accommodations, contact us promptly at recruitment@cancer.org.uk or call 020 3469 8400.

Eligibility: Candidates must have the legal right to work in the UK. Cancer Research UK cannot provide visa sponsorship for this role.

Recruitment Process: Includes a pre-prepared task followed by a competency-based interview.
Interview Week: Beginning 13 January 2025 (shortlisting will occur in December).

About Cancer Research UK
Our mission is to beat cancer.

We are seeking a talented Regulatory Medical Writer to join our innovative Centre for Drug Development (CDD). CDD is the world’s only charity-funded drug development centre, working to advance new treatments for cancer patients. As the sponsor of early-phase and precision medicine clinical trials, we operate with a portfolio comparable to that of a medium-sized pharmaceutical company, exploring areas such as antibodies, cell therapies, vaccines, drug conjugates, and small molecules.

This is a rare opportunity to contribute to pioneering research aimed at accelerating breakthroughs for cancer patients.

What You’ll Do

• Produce, edit, review, and ensure quality control of essential documents, such as clinical study reports and investigator brochures.
• Oversee the development of clinical study reports, collaborating with project teams to define requirements, assign responsibilities, and set production timelines. Contribute to the preparation and publication of clinical trial summaries and related disclosures.
• Coordinate the review and updates of investigator brochures in line with regulatory requirements, ensuring annual updates for active trials.
• Collaborate with project teams on specific tasks, including protocol reviews, Trial Master File evaluations, data analysis, and expert reports.

What We’re Looking For

• Proven experience in medical or scientific writing, with significant exposure to regulatory medical writing or a combination of regulatory writing and related roles in clinical trials, pharmacovigilance, or medical writing.
• A background in science (degree level or equivalent), coupled with substantial scientific writing expertise.
• Strong understanding of regulatory standards for clinical trial documentation, such as investigator brochures, clinical study reports, and clinical trial summary results.
• Meticulous attention to detail with excellent proofreading skills.
• Strong communication skills and the ability to build collaborative working relationships both internally and externally.
• Project management capabilities.
• While prior experience in early-phase oncology trials is advantageous, it’s not a requirement—we encourage you to apply regardless.

Our Values

We embody the following values to drive progress in our mission:

• Bold: Approach challenges with ambition, courage, and determination.
• Credible: Work with professionalism and rigour.
• Human: Make a meaningful and positive impact on people’s lives.
• Together: Foster inclusivity and collaboration.

If these values resonate with you and align with your aspirations, we’d love to hear from you—even if you’re unsure about meeting all the criteria.

What We Offer

Cancer Research UK is committed to supporting your wellbeing and career development. You’ll have access to a generous benefits package, diverse learning opportunities, and high-quality tools to help you achieve your personal and professional goals.

Visit our careers page for a comprehensive overview of our employee benefits.

Application Process

We utilize an anonymized shortlisting process to promote fairness and inclusion. While CVs are required, they will only be reviewed once you are shortlisted for an interview. Instead, we assess candidates based on the information provided in the work history section of the online application form.

For more information or assistance with the application process, please reach out to recruitment@cancer.org.uk.

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Our Commitment

Cancer Research UK prioritizes the safety and well-being of its staff, volunteers, and all others engaged with the charity. For more details, visit our safeguarding statement on our website.

We strive to create an environment where everyone feels included and can contribute to our mission. We strongly encourage applications from individuals of all backgrounds, especially those from underrepresented groups.

If adjustments or accommodations would enhance your experience during the application or interview process, please let us know by contacting us at recruitment@cancer.org.uk or calling 020 3469 8400.

Note: Due to safeguarding policies, applicants must be at least 18 years old.