- You will use your GCP auditing expertise, regulatory knowledge and excellent communication skills to support the audit programme
- As part of the role you will plan, conduct and follow-up a number of different audits including;
- The role will include both UK & International travel
- You will be expected to provide support, advice, education and training to other departments involved in clinical trials
- You will also set up, review and maintain the SOPs and support the development, maintenance and audit of documentation
- Bachelor degree in life-science
- Proven experience in a GCP and minimum 5 years experience in an auditing role
- Experience in the conduct of audits( Vendor audits, Investigator Site Audits, Process audits etc)
- Experience in clinical studies phase II-III
- Experience with EUand FDA regulations
- A full clean drivers license
- FTE: 1.0
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Clinical Quality Assurance UK - United Kingdom - Resourcing Life Science
Description
Company Description
Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a GCP Auditor /Clinical Quality Assurance Auditor based in UK.
Job Overview
Key Requirements
If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on or email -
Tagged as: qa jobs
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