Medpace is seeking a Clinical Research Monitor to conduct qualification, initiation, monitoring and closeout visits across research sites in compliance with the approved protocol. You will liaise with site staff, verify investigator qualifications, and ensure proper documentation, regulatory compliance, and drug accountability.
A Bachelor's degree in health/science and robust communication skills are essential.
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📌 Travel Ready Clinical Research Associate — Site Monitoring Melbourne (Australia)
🏢 Medpace
📍 Australia
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