IQVIA is seeking an in office Clinical Research Associate to monitor trial sites in Australia, ensure protocol adherence, and manage data submission. You will coordinate recruitment, maintain TMFs, and liaise with the study team to support start-up activities.
The role requires at least 2 years' CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS tools. Excellent communication and time management are essential.
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📌 Sponsor-Driven Clinical Research Associate (Melbourne)
🏢 Iqvia
📍 Melbourne
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