Worldwide Clinical Trials is seeking a TMF Records Management professional to support the Records Management Compliance Department in handling trial master file documents with accuracy and timeliness.
You will process, review, and resolve TMF documents, work with electronic systems, escalate quality issues, and provide admin support to the RMC Lead to help ensure regulatory compliance across studies. This role requires clear communication and meticulous data handling.
📌 TMF Operations Specialist I (Argentina)
🏢 Worldwide Clinical Trials
📍 Argentina
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