Associate Director of Clinical Quality Assurance
Blackfield Associates are partnered with a Global clinical trial testing organisation based in Yorkshire in the search for an Associate Director of Clinical Quality Assurance.
the Associate Director of Clinical Quality, your primary responsibility will be to enhance the effectiveness and efficiency of Quality and Operations, which involves streamlining processes on a global scale. Other key Responsibilities include:
- Supervise the day-to-day management activities of a regional Quality Assurance Team.
- Create and implement processes aimed at ensuring effective, efficient, and compliant clinical trials and lab operations.
- Establish and implement a comprehensive audit program that encompasses internal audits, vendor audits, client audits, and regulatory inspections to guarantee compliance.
- Offer ongoing coaching and mentorship, utilizing regular performance metrics, to discern specific performance feedback and formulate career development plans.
The correct candidate for this opportunity would have an extensive background working in a senior quality leadership role within Good Laboratory Practice (GLP) and Good Clinical Practice (GCP). Experience working with the FDA or MHRA is also highly desirable.