Hiring- FSP CTC II
Core
Administrative and technical support for clinical trial site activation, feasibility assessments, and audit readiness.
Role type
Mid-level Clinical Trial Coordinator (CTC)
Builds
Site activation critical paths, feasibility assessments, and regulatory compliance packages
Domain
Clinical Research / Pharmaceutical Trials
Deliverable
client delivery
Required skills
Site activation coordination, feasibility assessment, (e)TMF management, CTMS usage, regulatory document review, vendor management, site list development, data reconciliation
Preferred skills
Vendor management experience, global clinical trial coordination
Technologies
Veeva eTMF, CTMS, MS Office
Responsibilities
Coordinate site activation activities and critical path development; conduct feasibility assessments and develop site lists; manage (e)TMF and regulatory documents; support audit readiness and file reviews; maintain study metrics and database accuracy; train new personnel on processes.
Seniority
Mid-level, hands-on IC