Accelagen Pty Ltd invites applications for a Senior Clinical Research Associate to oversee site monitoring, from start-up through close-out, across diverse protocols and therapeutic areas. You will ensure data integrity and compliance while supporting regulatory processes.
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The role requires at least 3 years of in office monitoring experience, solid ICH-GCP knowledge, and the ability to travel interstate across Australia. You will mentor junior CRAs in a collaborative, fast-paced setting.
📌 Senior Cra Global Trial Site Monitoring Leader Victoria (Australia)
🏢 Accelagen
📍 Australia
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