Clinical Trials Programme Manager

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Key Information

Salary:Commencement on the salary range is subject to comparable skills and experience. Future progression is based on annual performance review.

Duration of Contract: Fixed Term for 3 years

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: 23 March 2025

Job Details

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.

The post offers an excellent opportunity for an enthusiastic and well-motivated senior trial manager with extensive experience of setting up and running multi-centre trials to work in a dynamic and supportive academic environment at one of the leading National Cancer Research Institute cancer trials units. The successful candidate will join the ICR-CTSU Management Group and responsibilities will include:

• 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.

We encourage all applicants to access the job pack attached for more detailed information regarding this role.

For an informal discussion regarding the role, please contact via Email on [email protected].

About The Institute of Cancer Research

Why work for us?

As a member of staff, you'll have exclusive access to a range of staff benefits.

The ICR is committed to supporting overseas applicants applying for roles, please click here to find out further information.

The Institute of Cancer Research, London, is one of the world's most influential cancer research institutes, with an outstanding record of achievement dating back more than 100 years. Further information about working at the ICR can be found here.

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.

Don't let a checklist of qualifications hold you back - if you're passionate about the role, we want to hear from you. Your unique experiences and backgrounds contribute to the richness of our team. We are committed to being an equal opportunity for all, regardless of ethnicity, gender, age, sexual orientation, disability, or any other dimension of diversity. Join us in creating an inclusive environment where everyone's voice is heard and valued.