Fortrea is seeking a Site Monitor to oversee clinical study sites, ensuring protocol adherence, data integrity, and audit readiness. The role involves visits, CRF review, and collaboration with vendors and internal teams.
The candidate should hold a Master’s degree, a CRA certification, and at least 1 year of independent monitoring experience, with fluency in Italian and English and a valid driver’s license.
📌 Junior Clinical Research Associate — Site Monitoring (Milano)
🏢 Fortrea
📍 Milano
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