FSP Clinical Trial Coordinator
Core
Administrative and technical support for clinical trial site activation, feasibility, and regulatory compliance across global projects.
Role type
Junior Clinical Trial Coordinator (Site Activation & Feasibility)
Builds
Site activation plans, feasibility reports, regulatory compliance packages, and study documentation.
Domain
Clinical Research / Pharmaceutical Services
Deliverable
client delivery
Required skills
Site selection and tiering, regulatory document review, (e)TMF management, study metrics analysis, local market knowledge, SOP adherence, risk escalation, stakeholder communication, MS Office proficiency.
Preferred skills
Bachelor's degree, prior clinical trial experience, knowledge of ICH GCP and country regulations.
Responsibilities
Coordinate site activation activities and develop critical paths; conduct file reviews and document findings; support feasibility visits and site list development; manage (e)TMF and study documentation; analyze study metrics and resolve findings; liaise with investigators and global teams; train new staff on processes and systems.
Seniority
Entry-level (0-1 years experience)