Fortrea is seeking a Site Monitor to oversee clinical studies in Argentina, ensuring adherence to SOPs, regulatory guidelines, and project plans. You will monitor sites, manage data integrity, and support site staff through monitoring visits. The role requires regulatory knowledge, English fluency, and the ability to work in a matrix environment, with travel as needed to sites and sites, and driving license preferred.
📌 Clinical Research Associate I: Site Monitor (Tandil)
🏢 Fortrea
📍 Tandil
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