Description
The Clinical Trial Associate will support clinical research projects by coordinating site personnel and CROs, resolving queries, completing EDC, managing vendors and clinical supplies, tracking CTMS issues, handling regulatory and ethics submissions, coordinating audits, maintaining TMF and Investigator Site Files, and supporting site training and safety information. The role is a hybrid opportunity in Bogotá and requires a life sciences degree, clinical research and CRO experience, English proficiency, MS Office skills, and knowledge of local regulations.
