Accqm
Job Location:
Maidenhead - UK
Monthly Salary:
Posted:
Application Deadline:
Vacancies:
Job Summary
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 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.
- 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 were looking for
- Bachelors 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. Youll 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.
