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CareersWe are currently seeking a Clinical Trial Administrator.


The Clinical Trial Administrator will provide administrative support to the technical aspects of the QRCC business and staff, including clinical and regulatory services.  The successful candidate will be based at our offices in St Ives, Cambridgeshire.


Qualifications and Experience

The Clinical Trial Administrator will ideally have relevant experience from working in a clinical development environment at either a CRO or a bio-pharma company and will have knowledge and understanding of GCP and the Trial Master File (paper and/or eTMF).  They will have competent word processing skills (including use of standard MS Office applications).


Reporting lines

The Clinical Trial Administrator will report to the Head of Clinical Operations for all technical issues and also for personnel matters. 


Technical roles and responsibilities

Outlined here are the tasks that will generally be the responsibility of the Clinical Trial Administrator, but they may be delegated to other staff where appropriate:


General responsibilities:


Working hours:

The role is flexible in terms of number of days per week; 3 days a week would be the minimum, with up to 5 days available.

 If interested please contact Pamela Ensor (pam.ensor@qrcc.co.uk; Tel 01480 309349)