IQVIA LLC is seeking a Clinical Research Associate to monitor study sites and ensure data reported aligns with protocol and regulatory requirements. You will manage site communications, train staff, and track regulatory submissions, recruitment, and data queries.
Milano-based, onsite role requiring strong English communication and organized project oversight. Experience with GCP/ICH guidelines and CRA certification is essential; opportunity to contribute to global clinical research operations
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📌 Clinical Research Associate: Site Monitoring (Milano)
🏢 Iqvia
📍 Milano