Principal GCP QA Consultant - Cambridgeshire

C.K. Associates Limited
Up to £75,000
13 Nov 2017
15 Nov 2017
Contract Type
Full Time
Jim Gleeson is recruiting for a permanent Principal Clinical QA Consultant for a well established and highly successful consultancy, based at their offices in Cambridgeshire.

As Principal Clinical QA Consultant you will provide clinical trial audit and QA support to a range of customers on a global basis.

Key duties will include:
- Audit plan preparation
- Execution and reporting of audits of systems, Phase I units, clinical laboratories, Investigator sites etc
- Preparation of SOPs for clients
- Preparation for agency inspections
- Training and mentoring of internal staff

As Principal Clinical QA Consultant you will require the following:
- A life science BSc
- Extensive GCP QA experience gained within the pharmaceutical industry
- GVP and GLP QA experience will be advantageous
- Excellent communication and IT skills
- Able to travel internationally on a regular basis

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL40536 in all correspondence.