FSP Clinical Trial Coordinator I
Core
Administrative and technical support for clinical trial site activation, feasibility, and regulatory compliance across global projects.
Role type
Clinical Trial Coordinator I (Site Activation & Feasibility)
Builds
Site activation critical paths, feasibility site lists, regulatory compliance packages, and study documentation systems.
Domain
Clinical Research / Pharmaceutical Services
Deliverable
client delivery
Required skills
Site selection and tiering, regulatory document review, (e)TMF management, study metrics analysis, vendor tracking, local market knowledge, SOP compliance, risk escalation, translation coordination, system administration.
Preferred skills
Bachelor's degree, 0-1 years experience, local language proficiency.
Technologies
Activate, eTMF, CTMS, MS Office, clinical trial database systems.
