Caidya is seeking a Senior Clinical Research Associate to monitor investigational sites and ensure high-quality data in compliance with GCP/ICH and ISO14155. The role acts as a liaison between Sponsor and sites, supporting regulatory submissions and site relations.
The Senior CRA will conduct routine visits, verify regulatory compliance, and ensure subject rights and safety throughout the trial lifecycle, while collaborating closely with the Project Team and CRO partners.
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📌 Senior Clinical Research Associate - Global Site Monitor (Brisbane City)
🏢 Caidya
📍 Brisbane City
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