{ “@context”: “http://schema.org”, “@type”: “JobPosting”, “title”: “Senior Clinical Study Project Manager”, “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
Company: Barrington James
Location:
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
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Posted: March 6th, 2026