Associate Director, Clinical Quality Assurance

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profile Job Location:

Hatfield - UK

profile Salary: Not Disclosed
Posted on: 2 days ago
Vacancies: 1 Vacancy

Job Summary

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...
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Company Industry

Pharmaceuticals


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Idibu

100 employees

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