Fortrea is seeking a regulatory affairs skilled to serve as the primary contact for investigative sites in Australia, ensuring timely collection of essential documents for IRB/IEC submissions and site activations.
You will support senior staff in compiling and submitting regulatory packages in accordance with local requirements and guidelines.
You will liaise with internal and external vendors, perform final document reviews, and maintain status updates.
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📌 Regulatory Submissions Specialist – Clinical Trials (New South Wales)
🏢 Fortrea
📍 New South Wales
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