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.
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
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📌 Clinical Trial Submissions & Site Activation Associate (City of Sydney)
🏢 FTSYD Fortrea Australia
📍 City of Sydney
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