Gcp Quality Assurance Auditor Contract

GCP Quality Assurance Auditor Contract – Cambridge

Opportunity:

Are you currently working in clinical research? Have you conducted GCP audits to clinical trials? Looking for a new opportunity with a growing well respected pharmaceutical company? Yes then this is the role for you.

Your role as a GCP Quality Assurance Auditor will involve conducting third party GCP audits to clinical studies and manage the design and implementation of the audit programme for the clinical development functions, including internal systems, external supplier and essential documentation and investigator site audits. You will also provide support, advice, education and training to other departments involved in clinical trials and pharmacovigilance activities and host GCP and pharmacovigilance regulatory inspections.

You will assist with the set up and maintenance of procedures within Clinical Development and support the development, maintenance and audit of marketing authorisation application dossiers.

This is a full time 2 year contract opportunity. This role involves around 40% travel within the UK and overseas.

Skills:

To apply for the role of GCP Quality Assurance Auditor you will have the following:

• Ideally a bioscience degree or nursing qualification.
• Proven experience in GCP investigator site auditing.
• A full driving licence is required along with the ability to travel approximately 40% of the time both within the UK and overseas.

How to Apply:

If this sounds like the role for you or a colleague then please don’t hesitate to contact us. Quality Start will offer £200 to anyone who successfully recommends a candidate who is subsequently employed by our client.

For a list of our current vacancies, please apply.

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.