Fortrea
Associate Country Clinical Quality Manager
Associate Country Clinical Quality Manager
Posted 3 weeks ago
LondonPermanentHybridFull-TimeMid-Level
Posted 3 weeks ago
Description
Associate Country Clinical Quality Manager (ACCQM)
Location: London, UK (Hybrid – 2 days per week in the office)
About the role
Fortrea is seeking an Associate Country Clinical Quality Manager to join our UK client-dedicated team. This role is particularly well suited to experienced SCRAs (ideally 4+ years’ experience) who are ready to transition into a more quality, compliance, and oversight-focused career path.
This is an excellent next step for professionals who have strong site monitoring experience and are passionate about driving quality, inspection readiness, and continuous improvement across clinical trials.
What you’ll do
What we’re looking for
Nice to have
At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.
Location: London, UK (Hybrid – 2 days per week in the office)
About the role
Fortrea is seeking an Associate Country Clinical Quality Manager to join our UK client-dedicated team. This role is particularly well suited to experienced SCRAs (ideally 4+ years’ experience) who are ready to transition into a more quality, compliance, and oversight-focused career path.
This is an excellent next step for professionals who have strong site monitoring experience and are passionate about driving quality, inspection readiness, and continuous improvement across clinical trials.
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
What we’re looking for
- Bachelor’s degree in a life sciences or healthcare-related field
- 4+ years’ experience as a CRA (or equivalent CRM role)
- Strong understanding of clinical trial conduct and GCP requirements
- Experience in site monitoring, 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
Nice to have
- Experience supporting compliance investigations or quality issue management
- Exposure to pharmacovigilance, privacy events, or serious breach reporting
- Previous involvement in inspection readiness activities
At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

