Worldwide Clinical Trials is seeking a Records Management Compliance professional to support TMF operations across multiple studies. The role involves processing and reviewing TMF documents, ensuring quality control, and collaborating with project teams to maintain regulatory alignment.
Candidates should have a life science background and up to 2 years of TMF experience, with strong skills in data handling, communication, and MS Word/Excel.
📌 TMF Operations Specialist II — Global Impact (Argentina)
🏢 Worldwide Clinical Trials
📍 Argentina
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