ICON plc in Australia seeks a Clinical Research Associate to conduct site qualification, initiation, monitoring and close-out visits for clinical trials. You will ensure protocol compliance, data integrity and patient safety while collaborating with investigators to facilitate study conduct.
The role requires a Bachelor’s degree in a scientific/healthcare field, at least 2 years as a CRA, thorough knowledge of ICH-GCP, excellent organization and communication skills, and the ability to travel
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📌 Global Clinical Research Associate - Trials & Monitoring (New South Wales)
🏢 ICON Strategic Solutions
📍 New South Wales
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