Medpace is seeking a Clinical Research Monitor to perform qualification, initiation, monitoring and closeout visits at study sites in Australia, ensuring adherence to the approved protocol and GCP standards.
The role involves coordinating with site staff, verifying investigator qualifications, and ensuring proper documentation, safety reporting, and regulatory compliance throughout all monitoring activities.
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📌 Clinical Research Monitor — Site Compliance & Data Integrity (New South Wales)
🏢 Medpace
📍 New South Wales
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