08 ott - Varese
Iqvia
IQVIA is seeking a Clinical Research Associate to perform site monitoring and ensure compliant data reporting per study protocol and regulations. The role involves monitoring visits, site training, and ongoing project communication across multiple sites in Italy.
The candidate should have a Master’s in a scientific field, 3+ years of on-site monitoring experience, and a CRA certification, with strong English communication and MS Office skills.
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