FSP Clinical Trial Coordinator
Core
Provide administrative and technical support for clinical trial site activation, documentation management, and operational oversight.
Role type
Clinical Trial Coordinator
Builds
Clinical trial site activation and documentation packages
Domain
Pharmaceutical/Biotech clinical research
Required skills
Document management, site activation support, clinical systems management, supplier coordination, regulatory compliance (ICH/GCP), tracking tools management
Preferred skills
Project prioritization, independent work, cultural-sensitive communication
Technologies
MS-Office (Excel, Word, PowerPoint, Outlook), Clinical systems, TMF/ISF
Responsibilities
Ensure timely availability of trial materials and documentation, Manage TMF and ISF setup and filing, Coordinate with suppliers for site supplies and logistics, Support site activities including feasibility and initiation readiness, Maintain tracking tools for operational oversight
Seniority
Entry-level, individual contributor
