PSI CRO Chile is seeking a dedicated Clinical Trial Assistant to support site personnel and CRA teams, handling documentation, queries, and EDC tasks to keep studies on track.
The role requires a life sciences degree, CTA experience in CROs, strong English, and proficiency with MS Office; you will coordinate regulatory submissions and TMF files.
Join our international research team and grow in clinical trials while contributing to high-quality study management.
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📌 Global Clinical Trials Site Coordinator (Chile)
🏢 Psi Cro
📍 Chile