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Ranges from single to multi-centre, national to international, phase II to phase IV drug trials, as well as other randomised control trials and well designed studies.

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Careers

People are the foundation of the CCTU's success. Build a career in a unit that supports life-changing clinical research.

We improve people's quality of life by supporting innovative and sustainable healthcare research to support safe, kind and excellent delivery of healthcare. We foster an inclusive culture that promotes equality of opportunity, values diversity and maintains a working environment in which the rights and dignity of all our staff are respected. Personal and professional development is key to enabling individuals to reach their full potential and maximise their contribution to the CCTU.

Applications are invited for the following post(s):

Clinical Trials Coordinator

Main area: Cambridge Clinical Trials Unit

Employer: Cambridge University Hospitals NHS Foundation Trust
Grade: Band 6 Employer Type: NHS

Contract: 24 months (Fixed Term for 24 months)

Site: Cambridge Biomedical Research Campus

Hours: Full time - 37.5 hours per week 

Town: Cambridge

Job ref: 180-RD-245295

Salary: £35,392 - £42,618 p.a.

Closing: 17/07/2024

Salary period: Yearly

Job overview:

An exciting opportunity has come up to join the Cambridge Clinical Trials Unit (CCTU).  The CCTU is a UKCRC Registered Clinical Trials Unit and caters for all investigators of Cambridge University Health Partners (CUHP), and beyond and has responsibility for new and existing clinical trials and clinical research projects on the CCTU portfolio, including Clinical Trials of Investigational Medicinal Products under the EU Directive (CTIMPS).

 

Main duties:

  • To facilitate and co-ordinate the set-up and conduct of clinical trials and/or clinical studies working closely with the chief investigators and their teams
  • To have responsibility for setting-up participating sites in multi-centre trials and ensuring that all data and samples are collected following the protocol
  • To work in compliance with the International Conference on Harmonisation Good Clinical Practice Guidelines (ICH-GCP), the NHS Research Governance Framework for Health & Social Care and, in the case of a CTIMP, in compliance with the Medicines for Human Use (Clinical Trials) Regulations 2004.

 

For more information and to apply online now