Medpace in Australia is seeking a Clinical Research Monitor to conduct qualification, initiation, monitoring, and closeout visits in line with the approved protocol. You will communicate with site staff, verify resources, and ensure adherence to GCP, SOPs, and regulatory requirements.
Responsibilities include reviewing regulatory documents, drug accountability, adverse event reviews, and supporting site recruitment.
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📌 Clinical Research Monitor & Compliance Specialist Queensland (Australia)
🏢 Medpace
📍 Australia
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