Worldwide Clinical Trials in Buenos Aires is seeking a Records Management Compliance professional to oversee TMF operations for globally sponsored studies. The role focuses on ensuring regulatory compliance, quality control, and timely data management across projects.
You will collaborate with project teams and sponsors, prepare KPI analyses, and support audits. A life sciences degree and 2–4 years of TMF or regulated-industry experience are preferred.
📌 TMF Operations Lead – Global (Buenos Aires)
🏢 Worldwide Clinical Trials
📍 Buenos Aires
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