ACCQM

Location: London, UK (Hybrid – 2 days per week in the office) Fortrea is seeking an Associate Country Clinical Quality Manager (ACCQM) to join our UK client-dedicated team. This role is ideal for an experienced clinical quality professional who understands country and site-specific risks and is passionate about driving quality, compliance, and inspection readiness. In addition to strong clinical quality expertise, we are looking for individuals who embrace digital and AI-enabled ways of working , using data, automation, and technology to improve quality oversight, risk management, and operational efficiency. As a trusted partner to country stakeholders, you will play a key role in safeguarding patient safety, data integrity, and regulatory compliance while helping to advance innovative, data-driven approaches to clinical quality management. What you'll do Partner with country stakeholders to identify, assess, and mitigate quality and compliance risks. Support audits and regulatory inspections, including CAPA development, root cause analysis, and follow-up activities. Act as a subject matter expert in ICH-GCP, regulatory requirements, and quality management frameworks. Support the implementation, maintenance, and continuous improvement of SOPs and quality systems. Identify trends, risks, and opportunities for process improvement through data-driven analysis and quality metrics. Leverage digital tools, reporting solutions, and automation opportunities to strengthen quality oversight and operational effectiveness. Contribute to inspection readiness activities and compliance monitoring. Support training, knowledge sharing, 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 Life Sciences, Healthcare, or a related field. Experience in clinical quality, compliance oversight, audits, inspections, or quality management activities. Experience with Power BI, Power Apps, automation tools, data analytics, or AI-enabled solutions . Exposure to audits, inspections, CAPA management, and quality investigations. Ability to identify risks, analyze trends, and drive continuous improvement. Interest in digital, data-driven, and AI-enabled approaches to quality management. Experience developing dashboards, metrics, or automated reporting. Nice to have experience as a CRA or in a similar clinical research role. Experience supporting compliance investigations or quality issue management. Exposure to pharmacovigilance, privacy events, or serious breach reporting. Previous involvement in inspection readiness activities. Why join us? This is an opportunity to combine clinical quality expertise with innovative digital and AI-enabled ways of working. You'll help drive quality, compliance, and inspection readiness while leveraging technology, automation, and data to improve clinical trial oversight. Learn more about our EEO & Accommodations request here .