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Clinical Trials Programme Manager

Institute of Cancer Research - Clinical Trials & Statistics Unit

Location: Sutton
Salary: £41,848 to £49,938 per annum
Hours: Part Time
Contract Type: Fixed-Term/Contract
Placed On: 6th August 2018
Closes: 3rd September 2018
Job Ref: 497
The Institute of Cancer Research, London, is one of the world’s most influential cancer research organisations, with an outstanding record of achievement dating back more than 100 years. We provided the first convincing evidence that DNA damage is the basic cause of cancer, and discovered many of the early chemotherapy drugs. Today, The Institute of Cancer Research (ICR) leads the world at isolating cancer-related genes and discovering new targeted drugs for personalised cancer treatment.

The ICR is ranked as the UK’s leading academic research centre. Our unique partnership with The Royal Marsden and ‘bench-to-bedside’ approach allows us to create and deliver results in a way that other institutions cannot. Together we are rated in the top four cancer centres globally.

The ICR is committed to attracting, developing and retaining the best minds in the world to join us in our mission – to make the discoveries that defeat cancer. 
  • Are you an experienced clinical trial/clinical project manager looking for a more strategic role? 
  • Are you motivated by the scientific rationale behind trials in cancer? 
  • Would you like to develop your career within a collaborative academic research environment? 

We are seeking an experienced trial manager to join the ICR-CTSU Management Group and provide strategic oversight to a defined programme of research within the ICR-CTSU portfolio. The successful candidate will play a key role in the development and initiation of new trials and will provide operational oversight of dedicated trials teams to ensure successful trial delivery.

Applicants should hold a first degree in a life science or health related subject and have an in depth understanding 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 a clinical trials unit, CRO or pharmaceutical company is essential. 

For more details please click on the link for the job description and person specification below. 

Appointment will be on a fixed term contract for 3 years.

To apply, please click on the Apply button below and follow the instructions.

When applying please provide a supporting statement as to why you are applying for this position and detailing your relevant experience; together with your CV including details of your current salary and the names and addresses of two referees.

Previous candidates need not re-apply.

Closing date for applications: 3 September 2018

Interviews are scheduled for w/c 17 September 2018

We consider all applications on merit and have a strong commitment to enhancing the diversity of our staff.

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