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
The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations. This includes site selection, initiation, monitoring, and close-out activities, while ensuring data