ICON plc is a world-leading healthcare intelligence and clinical research organization, dedicated to shaping the future of clinical development. Your role will involve delivering high-standard clinical trial monitoring work, coordinating activities with the team and stakeholders.
You will monitor studies, run sponsor-generated queries, and support cost efficiency, while building strong relationships with investigators and site staff. Travel of about 60% is expected.
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📌 Clinical Research Monitor: Trials (Italia)
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📍 Italia
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