Fortrea is seeking a Senior Clinical Research Associate to lead on-site monitoring and site management for clinical studies. You will ensure proper enrollment, data integrity, and adherence to regulatory guidelines, while coordinating with vendors and internal teams.
The role requires experience in SAE reporting, protocol development support, and the ability to travel 60–80% to sites. Solid English communication and organizational skills are essential.
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📌 Senior CRA – Site Monitoring Lead (Melbourne/Sydney)
🏢 Fortrea
📍 Melbourne
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