CRA II

Act as point of contact for Sites; Implements country/site feasibility; manages CTAgs and Master Service Agreements; prepares ICFs and site regulatory documents; coordinates Site Ethics submissions and EC/HA approvals; conducts site visits, qualification, initiation, and routine monitoring; ensures compliance with ICH GCP and local regulations; supports training of site staff; maintains relationships with internal/external stakeholders; supports drug accountability and trial documentation; contributes to risk-based monitoring strategies; works within BMS occupancy design for site-essential/hybrid/remote roles.