FSP Clinical Trial Coordinator II
Core
Administrative and technical support for clinical trial site activation, feasibility assessments, and regulatory compliance across global projects.
Role type
Clinical Trial Coordinator II (Central/Local)
Builds
Site activation critical paths, feasibility assessments, regulatory compliance packages, and study documentation.
Domain
Clinical Research / Pharmaceutical Services
Deliverable
client delivery
Required skills
Site activation coordination, feasibility assessment, regulatory document review, (e)TMF management, site list development, data reconciliation, vendor tracking, training support, meeting coordination, system administration
Preferred skills
Local market knowledge, strategic site tiering, on-site feasibility visits, RBM support, translation QC
Technologies
Activate & eTMF, CTMS, MS Office
Responsibilities
Coordinate assigned trial activities per task matrix; perform file reviews and document findings; process documents for (e)TMF; develop and review site lists for feasibility; conduct on-site feasibility visits (Asia Pac); train new personnel; support regulatory submissions and compliance reviews; maintain study metrics and database accuracy.
Seniority
Mid-level, hands-on IC