Teams at Fortrea

Perform site monitoring and site management for clinical studies: initiation, routine monitoring, closeout, source data and CRF review, SAE tracking, regulatory and consent compliance, vendor liaison, trip reporting, QC follow-up, registry and feasibility tasks, and support local project coordination and training under supervision.

Lead site identification and full start‑up activities, manage EC/RA submissions, oversee regulatory documents, negotiate site contracts and budgets, perform in‑house CRA tasks (remote monitoring, CRF/document review), ensure TMF inspection readiness, and coordinate with CRAs and cross‑functional teams to meet study timelines.

Provide on-site administrative support to the Japan Site Navigator team: printing, scanning, filing, preparing signature packages and binders, tracking shipments and approvals, maintaining study files, and supporting office operational tasks to reduce workload for site staff.