GCP Auditor - Contract

Requirements:

The organisation provides a comprehensive range of services in Phase I-IV clinical trials to the biopharmaceutical and device industries. The Lead QA Auditor will perform QA audits of clinical trial data and records in order to assure compliance.

Responsibility:

Planning and conducting regular and random QA audits in order to assure that clinical trials are of the highest standard and are in compliance with the requirements.
Perform quality system audits if required
Perform contract audits for Sponsor companies as required
Ensuring that audit results are formally recorded and reported and that corrective/preventive actions are documented
Assist with the development of the project audit procedures
Assist in training as appropriate

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Previous experience in GCP Quality Assurance auditing
Detailed knowledge of GCP guidelines and relevant regulations for the conduct of clinical trials

PERSONAL SKILLS & ATTRIBUTES:
Excellent communication and interpersonal skills
Coaching/mentoring skills
Good planning and organisational skills
Competent computer skills
Availability to travel at least 35% of the time (international and domestic)

If you are interested in this position and would like to hear more, please contact Hemish Ilangaratne on 020 7758 7322 or email with an updated CV. We also offer £200 worth of vouchers for any successful referrals.

Look forward to hearing from you.To find out more about Real please visit www.realstaffing.com