ICON is seeking a Clinical Research Associate to contribute to the design and analysis of clinical trials within sponsor-dedicated model. You will monitor sites, ensure protocol adherence, data integrity, and patient safety, and collaborate with investigators to ensure smooth study conduct.
You will review data, resolve queries, and help prepare study documents to support trial quality. The role combines hands-on monitoring with cross-functional teamwork to advance treatments for patients
📌 Clinical Research Associate: Site Monitoring (Torino)
🏢 Experteer Italy
📍 Torino
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