Clinical Trial Manager
$55,000–$75,000 year
HybridManchester, England, United Kingdom
Job Summary
Oversee clinical trial planning and implementation from protocol development through final study report for Phase I–IV trials. Lead cross-functional teams including CRAs, Data Management, Regulatory, and Biostatistics while managing CRO oversight. Develop study budgets, timelines, and site selection strategies. Monitor trial metrics, risk mitigation plans, and vendor performance to ensure compliance with ICH-GCP, MHRA, EMA, and FDA standards. Serve as the main point of contact for clinical sites, investigators, and stakeholders. Coordinate internal and external team meetings and status reports. Manage documentation and trial master files to inspection-ready standards. This role supports prestigious clients in delivering high-quality trials on time and within budget.
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
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