Fortrea Australia Pty Ltd is seeking a primary contact with investigative sites during study maintenance and site startup activities, ensuring regulatory documents are collected and submissions are made within timelines with project management.
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With guidance from senior staff, you will develop awareness of regulatory legislation and work with internal and external vendors to compile, submit, and obtain approvals from IRB/IEC/Regulatory Authority, maintaining audit readiness and explicit
📌 Clinical Trial Submissions & Site Activation Associate (New South Wales)
🏢 FTSYD Fortrea Australia
📍 New South Wales
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