Associate Country Clinical Quality Manager (ACCQM)
Location: London, UK (Hybrid – 2 days per week in the office)
Fortrea is seeking an Associate Country Clinical Quality Manager to join our UK client-dedicated team. This role is particularly well suited to an experienced Quality expert who understands country and site specific risks. The role partners with the country stakeholders to safeguard patient safety, data integrity and inspection readiness.
What you’ll do
- Support audits and regulatory inspections, including CAPA development and root cause analysis
- Act as a subject matter expert in ICH-GCP, regulatory requirements, and quality frameworks
- Support implementation and maintenance of SOPs and quality systems
- Identify trends, risks, and process improvement opportunities across studies
- Contribute to inspection readiness activities and compliance oversight
- Support training and quality awareness initiatives across teams
Assist with Quality Control activities, including site-related quality reviews where required
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What we’re looking for
- Bachelor’s degree in a life sciences or healthcare-related field
- Strong understanding of clinical trial conduct and GCP requirements
- Experience in quality oversight, or compliance activities
- Exposure to audits, inspections, or CAPA processes (highly desirable)
- Strong analytical thinking and problem-solving skills
Ability to work cross-functionally and manage competing priorities
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Nice to have
- 4+ years’ experience as a CRA (or equivalent CRM role)
- Experience supporting compliance investigations or quality issue management
- Exposure to pharmacovigilance, privacy events, or serious breach reporting
- Previous involvement in inspection readiness activities
Learn more about our EEO & Accommodations request here .
