In this SMA II role, you support the management and monitoring of clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP. You coordinate monitoring activities, assist in regulatory document preparation, and collaborate with cross-functional teams. You track site performance and provide reports to improve site management. You also participate in training initiatives and mentor junior staff, contributing to a values-driven, patient-focused research environment.
📌 Site Management Associate Ii (Milano)
🏢 Altro
📍 Milano