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](https://careers.fortrea.com/us/en/eeo-and-accommodations).