Fortrea seeks a Site Monitor to manage clinical study sites, ensuring protocol adherence, data integrity, and timely reporting. The role involves on-site monitoring, initiation/closeout visits, and liaising with vendors under SOPs and regulatory guidelines.
The candidate should have a related degree and at least 6 months of experience, with proficiency in English and computer tools, and a valid driver's license for travel as required.
📌 Junior Clinical Research Associate: Site Monitoring (Buenos Aires)
🏢 Fortrea
📍 Buenos Aires
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