Fortrea is seeking a Senior Clinical Research Associate I to oversee and monitor clinical trial sites, ensuring compliance, data integrity, and patient safety across studies.
You will collaborate with investigators, sponsors, and internal teams, travel *****% to sites, mentor junior staff, and help deliver high-quality data and study milestones.
The role requires a life sciences background, 3+ years of onsite monitoring experience, and solid regulatory knowledge.
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📌 Senior Cra I - Lead Site Monitor (60-80% Travel) (New South Wales)
🏢 Fortrea
📍 New South Wales
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