Clinical Trial Coordinator
Core
Coordinate clinical trial activities, manage documentation, and support site activation and regulatory submissions for clinical studies.
Role type
Clinical Trial Coordinator
Builds
Clinical trial documentation, site files, and regulatory submissions
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
eTMF management, site file review, regulatory documentation tracking, study coordination, risk identification, data entry accuracy
Preferred skills
ICH-GCP knowledge, Italian language proficiency, Microsoft Office proficiency, clinical trial system navigation, multi-tasking
Technologies
eTMF, Activate, clinical trial databases
Responsibilities
Coordinate assigned clinical trial activities per study task matrix, review country and investigator files, support audit readiness, process and maintain eTMF documentation, assist with site activation and start-up, transmit documentation to IRBs/IECs, support Risk-Based Monitoring activities, communicate site-related issues to project leads
Seniority
Entry-level to Mid-level, hands-on IC
