Senior GCP QA Auditor

Hobson Prior are currently working with a regulatory and clinical research organisation who is seeking a Senior GCP QA Auditor to join them on a permanent basis. You will provide QA audit and clinical research consultancy support to the organisation's clients.

Job Responsibilities:

• Conduct of CRO GCP systems audits, Phase I-unit audits and laboratory GCLP audits
• Conduct of clinical site audits (GCP).
• Clinical trial audit plan preparation.
• Agency inspection preparation; conduct of mock inspections.
• Conduct of QC reviews of essential documents.
• Training and mentoring of staff.
• Speaking at external meetings and conduct of client training seminars.
• Supporting clients as QA consultant.
• Supporting internal QMS activities including conduct of internal audits of the company's systems.
• Leading the business operations for QA services within the organisation.

Requirements:

• Life Science Degree (BSc) (minimum).
• Relevant experience from working in clinical drug development, including auditing and an understanding of the regulatory environment for conducting clinical trials.
• Competent Word Processing Skills (including use of standard MS Office applications).

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.