OPIS S.r.l. is seeking a Clinical Research Associate to manage and monitor clinical trials in compliance with study protocols, ICH-GCP and applicable regulations.
The role includes site selection, initiation, monitoring and close-out activities, while ensuring data quality and patient safety. The successful candidate will conduct feasibility, pre-study, initiation, monitoring visits, perform SDV, monitor recruitment, and support sites to meet targets.
J-18808-Ljbffr
📌 Clinical Research Associate: Lead Global Trial Monitoring (Italia)
🏢 Altro
📍 Italia