Associate Director, Clinical Quality Assurance

CK Group are recruiting an Associate Director, Clinical Quality Assurance, for a leading global pharmaceutical company. This hybrid role requires three days per week in their Home Counties office.

The Role:

As Associate Director, Clinical Quality Assurance, you will oversee GCP activities in-house, with CROs and at Investigator sites, lead GCP audits and manage inspection activities, ensuring the highest standards of quality compliance in all aspects of clinical research.

Responsibilities:

• Acting as CQA Lead for clinical studies, drafting and managing Audit Plans and Reports.
• Performing Clinical Investigator Site Audits, GCP Document Audits, Internal Process Audits and Vendor / System Audits.
• Leading regulatory authority inspection activities.

• Facilitating ongoing quality improvement.
• Representing the CQA group in internal meetings.
• Providing GCP training sessions for business groups.

• A relevant BSc.
• Strong Clinical Quality Assurance experience.
• Experience of performing internal and external audits and of hosting regulatory authority inspections.
• An in-depth knowledge of international regulations and guidelines for the conduct of clinical trials.
• Strong interpersonal skills.
• Ability to travel up to 25%.

Competitive salary plus an excellent benefits package.

Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference 169109 in all correspondence.