Clinical Trial jobs in United Kingdom

Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Precision for Medicine is expanding its European team and seeking a Manager of Clinical Monitoring (GCM) to lead and develop its Clinical Research Associates (CRAs). This role is vital for delivering high-quality monitoring services across global clinical trials, particularly in oncology, and requires fluency in both English and French. The role focuses on people management, strategic resourcing, training, and operational excellence.

• Mentor, lead, and manage a team of CRAs across multiple countries
• Support CRA career growth, performance reviews, and ongoing development
• Ensure CRAs are well-equipped with training, tools, and system access
• Monitor resourcing needs and allocate appropriate personnel to projects
• Collaborate with CTMs and Clinical Team Leads to meet project and site expectations
• Conduct accompanied site visits to assess CRA performance and development
• Lead improvement initiatives and develop strategic action plans for quality and efficiency
• Track CRA-related metrics and participate in system improvement planning
• Participate in CRA recruitment, CV screening, interviews, and onboarding
• Manage CRA compliance with administrative systems and SOPs
• Present and communicate effectively across stakeholders, including clients and internal leadership
• Contribute to departmental goals while maintaining a high standard of professionalism and emotional intelligence

• Bachelor's or equivalent in a scientific or healthcare field
• Fluent in English and French
• 7+ years in clinical operations or data management, including 5+ years of onsite CRA monitoring experience
• Strong oncology trial experience
• 3–5 years in a direct supervisory/management role of CRAs
• Demonstrated experience in creating CRA development programs and conducting performance evaluations
• Availability for international and domestic travel (approx. 25%)
• Mastery of ICH-GCP, local regulatory requirements, CRA SOPs, remote monitoring, and EMR/EDC systems
• Strong leadership and interpersonal skills
• Passion for people development and emotional intelligence
• Ability to identify training gaps and improve team effectiveness
• Highly organized with strong problem-solving and continuous improvement focus
• Comfortable delivering formal presentations to internal and external audiences

• Remote-based role with travel
• High focus on people leadership and project resource optimization
• Strong potential for career growth within an expanding global clinical organization