IQVIA is seeking an Experienced Clinical Research Associate, Site to perform monitoring and site management duties needed to ensure studies are conducted according to protocol, GCP, ICH guidelines, and sponsor requirements. You will conduct site visits—from selection to close-out—and ensure timely data reporting and regulatory compliance.
The role requires thorough understanding of monitoring processes and data integrity, with responsibilities spanning initiation, ongoing monitoring, and
📌 Site Monitoring Specialist – Clinical Research Associate (Roma)
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📍 Roma
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