FSP Clinical Trial Coordinator - Site Record Coordination
Core
Oversee the collection, review, tracking, and maintenance of essential study documentation to ensure accurate, timely, and compliant trial execution.
Role type
Clinical Trial Coordinator (Site Record Coordination)
Builds
Trial Master File (TMF/eTMF) activities, clinical systems, regulatory documentation, and site communications
Domain
Clinical research / Pharmaceutical
Required skills
Site documentation management, Clinical trial record coordination, Study lifecycle management, TMF/eTMF management, Regulatory documentation handling, Cross-functional stakeholder communication
Preferred skills
International clinical trials expertise, Quality-focused operational mindset
Technologies
Clinical systems, TMF/eTMF platforms
Responsibilities
Collect, review, track, and maintain essential study documentation, Support Trial Master File (TMF/eTMF) activities, Coordinate with clinical study teams, investigators, and research sites, Ensure adherence to clinical research standards
Seniority
Individual Contributor