IQVIA in Australia seeks a Clinical Research Associate to perform site monitoring and site management to ensure studies comply with protocol, GCP/ICH, and sponsor requirements. You will support site activities across Melbourne and Sydney, operating in a hybrid work setting with regular site visits.
The role emphasizes training, communication with sites, data integrity, and regulatory tracking, with opportunities to advance across trials and locations within IQVIA's global CRO network.
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📌 Clinical Research Associate — Hybrid Trials (Melbourne/Sydney)
🏢 Iqvia
📍 Sydney