Milan, Italy Full time R1575628 Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions: - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and Internatio…
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy
Iqvia
IT
🎯 Intermedio🧭 Other🏢 Sanità🗣️ Italiano
Competenze richieste
gcpclinical researchsite management
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