PIQVIA 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.br/Scorra la pagina per visualizzare tutti i requisiti del lavoro e le responsabilità che i candidati selezionati dovranno assumersi.br/You will conduct monitoring visits, manage recruitment plans, and coordinate with site staff, with IQVIA's global leadership in clinical research services.br/The role requires xysqume solid GCP/ICH knowledge, 3+ years on-site monitoring experience, and strong communication skills in English; proficiency /p #J-18808-Ljbffr
📌 Senior cra: site monitoring & study oversight (Milano)
🏢 Iqvia
📍 Milano