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
- 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
Learn more about our EEO & Accommodations request here.
Skills Required
- Bachelor's degree in life sciences or healthcare
- 4+ years' experience as a CRA or equivalent 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
- Strong analytical thinking and problem-solving skills
- Ability to work cross-functionally and manage competing priorities
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
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