Worldwide Clinical Trials seeks a Clinical Research Associate to oversee site qualification, initiation, monitoring, and close-out visits within Argentina. You will ensure patient safety, data quality, and regulatory compliance while coordinating with investigative sites and sponsor teams.
The role requires MD/Pharmacy or equivalent degree with CRA experience, strong knowledge of GCP/ICH or FDA/EU regulations, and proficiency with EDC systems, MS Office, and IxRS.
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📌 Senior Clinical Research Associate — Remote, Global Trials (Tandil)
🏢 Worldwide Clinical Trials
📍 Tandil
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