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.
Your Background:- 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%.
Salary: 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.
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 CR...
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.
Your Background:- 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%.
Salary: 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.
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