Fortrea Australia is seeking a Site CRA/Coordinator to monitor and manage clinical study sites, ensuring regulatory compliance and data integrity. The role covers routine monitoring, site initiation, and closeout visits, with travel requirements as an essential function of the job.
Responsibilities include training staff, coordinating with vendors, ensuring proper site budgets, and maintaining study documentation in line with SOPs and regulatory guidelines.
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📌 Clinical Research Associate I - Site Monitoring & Study Impact (New South Wales)
🏢 FTSYD Fortrea Australia
📍 New South Wales
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