Medpace Adelaide is seeking a Clinical Research Coordinator to support site monitoring activities across ongoing studies.
You will conduct qualification, initiation, monitoring, and closeout visits, ensure GCP compliance, verify investigator qualifications, and maintain accurate source documentation.
This role requires a health or science degree and tends to prefer at least 1 year of study coordination experience, with solid communication and regulatory knowledge.
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📌 Clinical Research Site Monitor: Impact & Compliance (Adelaide)
🏢 Medpace
📍 Adelaide
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