Senior Clinical Study Project Manager

Key Responsibilities

• 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:

• Medical device clinical investigation experience
• 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
• Learning & development opportunities
• Family-friendly policies
• Employee Assistance Programme (EAP)
• Strong wellbeing and ESG focus
• Supportive, collaborative team environment

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