Clinical Trial Manager
$55,000–$75,000 year
HybridLondon, England, United Kingdom
Job Summary
Oversee clinical trial planning and implementation from protocol development through final study report, leading cross-functional teams and managing CRO oversight. Develop and manage study budgets, timelines, and site selection while monitoring trial metrics, risk mitigation plans, and vendor performance. Ensure quality and regulatory compliance with ICH-GCP, EMA, MHRA, and FDA standards by serving as the main point of contact for clinical sites, investigators, and stakeholders. Coordinate internal and external team meetings, status reports, and documentation to maintain trial master files at inspection-ready standards. This role supports global, multi-centre trials with flexible hybrid working options.
Required Qualifications
- Extensive understanding of clinical trial regulations, GCP, ICH, and MHRA requirements
- Proven experience managing global or multi-site clinical studies
- Excellent leadership, team coordination, and stakeholder management skills
- Strong command of trial budget and vendor oversight
- Proficient with EDC systems, CTMS, and MS Office tools
Desired Qualifications
- Life sciences or health sciences degree (BSc, MSc, or equivalent)
- ACRP, SOCRA, or equivalent clinical research certification
- Experience with oncology, rare disease, or CNS trials
- Familiarity with EU CTR and decentralised trial models
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.