FSP Prin Clinical Trial Coordinator

About the role

Responsible for coordinating and supporting end-to-end clinical trial activities, ensuring operational excellence, regulatory compliance, and timely study execution. Works closely with CTLs, CTMs, investigators, vendors, and cross-functional teams to manage trial documentation, systems, reporting, and stakeholder communication.

What you'll do

• Coordinate and track study activities, timelines, and deliverables
• Maintain and review eTMF/TMF, CTMS, study trackers, and trial documentation
• Support regulatory submissions, audit readiness, and compliance with ICH-GCP and SOPs
• Schedule meetings, prepare meeting minutes, and facilitate communication across study teams
• Manage study supplies, investigator files, vendor trackers, and trial systems

What you need

• 6–11 yrs of experience
• Clinical research
• Documentation
• Regulatory affairs
• Communication
• SOP writing
• Any graduate