Job Description
Medpace is seeking a Clinical Research Associate to conduct site visits (qualification, initiation, monitoring, closeout) across nationwide locations with up to 80% travel. You will verify investigator credentials, review regulatory documents, and ensure data integrity per protocol and GCP.
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Robust communication, time management, and attention to detail are essential. The role requires a health/science background and likely 1 year of study coordinator experience.
📌 Clinical Research Associate Travel‐focused Site Monitoring Victoria
🏢 Medpace
📍 Victoria
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