IQVIA is seeking a Clinical Research Associate to monitor sites in Lombardia and ensure study data is collected per protocol and regulations. You will conduct visits, train site staff, and liaise with the study team to resolve issues and maintain high-quality data. The role requires a scientific degree, CRA certification, pharma/clinical trial experience, and willingness to travel. Strong English, organizational skills, and proficiency in MS Office are essential.
📌 Senior CRA — Site Monitoring (Como)
🏢 Iqvia
📍 Como