Own end-to-end project delivery of clinical studies and investigations
Act as primary liaison with sponsors, investigators, and clinical operations teams
Ensure compliance with GCP, ICH, ISO 14155, and applicable EU/US regulatory frameworks
Oversee financial performance, risk management, and resource planning
Supervise and support cross-functional project teams
Contribute to proposals, bids, and client meetings
Champion quality, innovation, and continuous improvement
Mentor junior team members and support departmental growth
About You 8+ years of clinical research experience
4+ years in demonstrable project management roles (CRO, pharma, or biotech)
Strong knowledge of GCP, ICH, and ISO 14155
Proven experience managing study budgets and financial oversight
Experience delivering studies on time and within budget
Confidence working independently while fostering a collaborative team culture
Strong technical skills (Microsoft Suite, CTMS, PM tools)
Nice to Have International regulatory experience
What’s On Offer Competitive base salary + performance-based bonus
Generous annual leave (including your birthday off)
Private medical insurance
Remote-first culture with flexible working
Professional memberships covered
Family-friendly policies
Employee Assistance Programme (EAP)
Strong wellbeing and ESG focus
Supportive, collaborative team environment
Senior Clinical Study Project Manager in London employer: Barrington James
Barrington James is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in Epidemiology and Real-World Evidence. With a strong emphasis on employee growth, we offer tailored development opportunities and the chance to lead impactful projects across diverse therapeutic areas in the dynamic UK/Europe market. Join us to be part of a team that values flexibility, creativity, and meaningful contributions to healthcare advancements.
