IQVIA is seeking a Clinical Research Associate to monitor sites in Lombardia and ensure study data is collected per protocol and regulations.
Non aspetti a candidarsi dopo aver letto questa descrizione: per questa possibilità è previsto un elevato volume di candidature.
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.
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Strong English, organizational skills, and proficiency in MS Office are essential.
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📌 Senior Cra — Site Monitoring & Management (Bardi)
🏢 Iqvia
📍 Bardi