Medpace in Australia is seeking a Clinical Research Monitor to conduct site visits per protocol, ensure data integrity, and uphold regulatory compliance. You will liaise with site staff, verify qualifications and training, monitor safety events, and manage drug accountability.
The role emphasizes adherence to GCP, SOPs and timely monitoring reports, with collaboration across cross‑functional teams to secure high quality data in clinical studies.
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📌 Clinical Research Monitor - Site Oversight & Compliance (Adelaide)
🏢 Medpace
📍 Adelaide
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