FSP Clinical Trial Coordinator
Core
Administrative and technical support for clinical trial site activation, feasibility, and regulatory compliance across pharmaceutical and biotech projects.
Role type
Clinical Trial Coordinator (Site Activation & Feasibility)
Builds
Site activation critical paths, feasibility plans, and regulatory compliance packages for clinical trials.
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 adherence, risk escalation, training delivery
Preferred skills
Bachelor's degree, 0-1 years experience, local language proficiency
Technologies
Activate, eTMF, CTMS, MS Office
Responsibilities
Coordinate site activation activities and feasibility visits; review and process regulatory and site files; manage (e)TMF and system databases; analyze study metrics and resolve documentation findings; support regulatory submissions and compliance reviews; train new staff on processes and systems.
Seniority
Entry-level, hands-on IC