GCP Specialist/Supervisor - £40K

Job Ref:	6168
Position:	GCP Specialist/Supervisor
Category:	Clinical - Quality Assurance
Basic:	£40000
OTE:	£
Location:	West & Wales
Description:	Become known as a specialist in GCP and travel the world! As part of a small but highly focused team you will travel internationally to conduct GCP audits of study sites participating in phase II-IV clinical trials. The travel will mainly be in Europe but could also include countries in the Asia Pacific region. This isn't just an auditing role, you will also act as Project Leader for clinical QA projects with responsibilities for contract/quality plan execution, pricing/budget management and timelines for clinical deliverables. There is also a strategic element to this job in that you will be the person responsible for developing quality management plans and then ensuring they are implemented. Essentially this is an office based role along the M4 corridor although for the right candidate home working is a possibility. Who should apply? You must have experience of auditing study sites to GCP within the CRO, pharma or academic environment. Exposure to documentation, system, process and facility auditing is desirable. If you are looking for a more varied quality monitoring role that can lead to management quickly, give us a call for more information!
Consultant:	Diane Elliott
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