At a Glance
- Tasks: Oversee clinical trials and lead dedicated teams to ensure successful delivery.
- Company: Join the Institute of Cancer Research, a leader in innovative cancer research.
- Benefits: Competitive salary, flexible working options, and exclusive staff benefits.
- Other info: Diverse and inclusive workplace committed to equality and innovation.
- Why this job: Make a real impact in cancer research while developing your career.
- Qualifications: Degree in life sciences or health-related field with clinical trials experience.
Salary From £50,825 per annum. Commencement on the salary range is subject to comparable skills and experience.
Duration of Contract: Fixed Term for 24 months
Hours per week: 35 hours per week (Full Time or Part Time minimum of 60% FTE), flexible working options may be considered.
Location: Sutton
Closing Date: 19 July 2026
Sponsorship: This role is eligible for ICR Sponsorship. If this is your first visa in the UK, support will be provided for costs associated with Visa application. If you are considering relocating to the UK, further information can be found.
Role Summary: The Institute of Cancer Research is looking for an experienced trialist to join the Cancer Research UK Clinical Trials & Statistics Unit (ICR-CTSU) as a Clinical Trials Programme Manager at its Sutton site in Surrey. ICR-CTSU runs a diverse portfolio of national and international phase III multi-centre randomised controlled trials, and phase II targeted treatment trials, with a special emphasis in breast, urological, lung and head and neck cancer treatments.
Responsibilities:
- The strategic oversight of a defined programme of research within the ICR-CTSU portfolio;
- The development and initiation of new trials;
- Providing operational oversight of dedicated trials teams to ensure successful trial delivery.
Key Requirements: Applicants should hold a first degree or equivalent level qualification in life science or health related subject and have an in depth understanding of the UK Clinical Trials Regulations, principles of Good Clinical Practice, Data Protection, Research Governance and the Human Tissue Act. Experience/knowledge of laboratory quality systems and procedures is highly desirable. Excellent interpersonal skills are required, as is the ability to work to high standards across a variety of tasks with constant regard to scientific and regulatory requirements. A proven track record in the planning, coordination and conduct of clinical trials within the NHS or academia, a CRO or a pharmaceutical company is essential.
Additional Information: This is an office based role. Requests for hybrid working (splitting time between our Sutton site and home) may be considered following successful completion of key training and if the role allows. Flexible working options may be considered.
Benefits: As a member of staff, you'll have exclusive access to a range of staff benefits.
Equality and diversity: At the Institute of Cancer Research, we champion diversity as we believe it fuels innovation and drives impactful research. We welcome applicants from all walks of life, valuing diverse perspectives that enrich our work. We are committed to being an equal opportunity for all, regardless of ethnicity, gender, age, sexual orientation, disability, or any other dimension of diversity.
Clinical Trials Programme Manager in Sutton employer: The Institute Of Cancer Research
The Institute of Cancer Research is an exceptional employer, offering a dynamic work environment in Sutton, Surrey, where innovation and collaboration thrive. With a strong commitment to employee growth, we provide access to exclusive benefits and flexible working options, ensuring a healthy work-life balance. Our dedication to diversity and inclusion fosters a culture where every voice is valued, making it a rewarding place for professionals passionate about advancing cancer research.
Contact Details:
The Institute Of Cancer Research Recruitment Team
