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Cheshire   •  Negotiable  •  Contract/Temporary, Full time


6 month contract

200 per day

Cheshire based

Cpl are seeking an experienced CTA/CRA who can support a leading academic institute with a UK wide Oncology study. This role will require you to be based in Cheshire 5 days per week, with potential travel 2/3 times per month to sites within England.

The successful CRA will have a strong knowledge of clinical trials research and experience of managing clinical documentation. You will have excellent organisational and planning skills, ideally with experience working within Oncology.

Key responsibilities shall include:

Liaise with the clinical sites to ensure all documents required are present

Verification of the CTMS

Reconciling paper and electronic documents

Organising consent forms and ICFs

Tracking and documenting case report forms (CRFs)

Ensuring al documentation is consistently tracked

Possibility of 2-3 on-site monitoring visits a month

Experience required:

Previous experience working within an academic institute

Strong knowledge of clinical documentation

Understanding of clinical processes and procedures

Worked as a CRA on-site or remotely

Ability too travel to Cheshire daily (parking is available on site)

If this role is of interest to you then please apply here or send your CV to sarah.phillips@cpl.com.

  • Agency: Cpl Life Sciences
  • Contact: Sarah Phillips
  • Reference: JO-2111-480238
  • Posted: 16th November 2021
  • Expires: 14th December 2021

Cpl Life Sciences

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