Coordinate day-to-day activity across multiple clinical studies, including complex and multi-site trials
Track timelines, milestones, and deliverables across competing priorities
Support study execution end to end, keeping work moving and visible
Step in as the client contact when the Project Manager is unavailable
Attend and contribute to client and internal study meetings
Respond to client questions with a clear understanding of study status
Draft core study documents such as Project Management Plans, Communication Plans, Risk Registers, and Training Matrices
Review protocols and budgets to define documentation and TMF requirements
Maintain TMF completeness, trigger milestones, and coordinate document uploads
Build and maintain trackers, task lists, and study logs
Manage changing priorities and align timelines with Project Managers
Create bespoke trackers or tools when clients request non-standard reporting
Mentor and support Associate PCs and PCs in their day-to-day work
Act as a senior team member, supporting colleagues and sharing best practice
Contribute ideas to improve processes and how the team works together
Requirements
Degree in healthcare / life sciences
Several years of hands-on experience coordinating clinical trials within a CRO, hospital-based research or academic research environment, as PC, study coordinator or similar
A solid understanding of how clinical studies are set up, delivered and maintained
Experience supporting or drafting study documents such as project plans, communication plans, trackers, or logs
Ability to read clinical trial protocols and extract key information to support study delivery
Working knowledge of TMF requirements and how documentation aligns with study milestones
Senior-level ways of working
Confidence communicating with clients and internal teams about study status and next steps
Comfortable working independently across multiple studies with competing priorities
Experience mentoring or supporting less experienced colleagues within a study team.