FSP CRA II（Wuhan）

A Clinical Research Associate responsible for site management and monitoring of clinical trials to ensure compliance with Fortrea SOPs, ICH GCP, and sponsor/regulatory requirements. The role includes conducting pre-study, initiation, routine, and close-out visits, source document verification, eCRF review, and management of investigational product accountability. The position requires frequent travel to study sites (approximately 60%) and collaboration with study teams to maintain data integrity and audit readiness.