Clinical Research Associate: Site Monitoring
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IQVIA LLC is seeking a Clinical Research Associate to monitor study sites and ensure data reported aligns with protocol and regulatory requirements.
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You will manage site communications, train staff, and track regulatory submissions, recruitment, and data queries. xbvzest
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