Worldwide Clinical Trials in Mexico City seeks a TMF Records Management professional to lead TMF operations within a regulated CRO setting. You will ensure quality, compliance and timely archival of essential clinical trial documents, collaborating with integral teams and Sponsor counterparts.
The role requires a degree in Life Sciences, 2–4 years’ experience in regulated environments, and strong communication to support audits and regulatory inquiries across the project lifecycle.
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📌 Senior TMF Operations Specialist, EMEA/LATAM (Ciudad de México)
🏢 Worldwide Clinical Trials
📍 Ciudad de México
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