IQVIA LLC is seeking a Clinical Research Associate responsible for site monitoring and study management to ensure protocol adherence, data quality, and regulatory compliance across assigned sites in Italy.Scorra la pagina per visualizzare tutti i requisiti del lavoro e le responsabilità che i candidati selezionati dovranno assumersi.You will conduct monitoring visits, manage recruitment plans, and coordinate with site staff, with IQVIA's global leadership in clinical research services.The role requires xysqume solid GCP/ICH knowledge, 3+ years on-site monitoring experience, and strong communication skills in English; proficiency
📌 Senior Cra: Site Monitoring & Study Oversight (Milano)
🏢 Iqvia
📍 Milano