FSP Clinical Trial Coordinator II
Core
Coordinate and facilitate project activities for clinical trials, serving as a cross-functional liaison and study lead.
Role type
Clinical Trial Coordinator II
Builds
Clinical trial documentation, regulatory submissions, and project tracking systems
Domain
Clinical research / Pharmaceutical services
Required skills
Project coordination, regulatory document review, data analysis, system administration, vendor management, ICH GCP knowledge
Preferred skills
Bachelor's degree, 4+ years experience, local language proficiency
Technologies
GoBalto, eTMF, MS Office, clinical trial database systems
Responsibilities
Coordinate assigned trial activities per task matrix, perform file reviews (department/Internal/Country/Investigator), ensure tasks are on time/budget/quality, maintain study documentation and (e)TMF, support RBM activities, process documents for clients and IRB/IEC, analyze study metrics, maintain vendor trackers.
Seniority
Mid-level, hands-on IC
