Senior Clinical Study Project Manager

Barrington James; England; Remote; GBP 70,000 - 110,000; Full time

Benefits offered by this job

Competitive base salary

Performance-based bonus

Generous annual leave

Private medical insurance

Flexible working

Professional memberships covered

Employee Assistance Programme

Employee Assistance Programme (EAP)

Wellbeing and ESG focus

Job summary

A leading clinical research firm in the United Kingdom seeks an experienced project manager to oversee end-to-end delivery of clinical studies. You will act as a liaison with sponsors and investigators, ensuring compliance with regulations. The ideal candidate has over 8 years of clinical research experience and strong project management expertise in CRO, pharma, or biotech settings. This role includes competitive compensation and offers a remote-first culture with robust employee support policies.

Qualifications

• 8+ years of clinical research experience.
• 4+ years in project management roles in 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.

Responsibilities

• Own end-to-end project delivery of clinical studies.
• Act as primary liaison with sponsors and investigators.
• Ensure compliance with regulatory frameworks.
• Oversee financial performance, risk management, and resource planning.
• Supervise and support cross-functional project teams.
• Contribute to proposals, bids, and client meetings.

Skills

Clinical research experience

Project management

Knowledge of GCP

Financial management

Team collaboration

Technical skills

Tools

Microsoft Suite

CTMS

Project Management tools

Job description

• 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