Regulatory Submissions Specialist - Clinical Trials (New South Wales)

Regulatory Submissions Specialist - Clinical Trials (New South Wales)

21 Sep
|
Fortrea
|
New South Wales

21 Sep

Fortrea

New South Wales

Job Description

Fortrea is seeking a regulatory affairs qualified 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.

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You will liaise with internal and external vendors, perform final document reviews, and maintain status updates.

📌 Regulatory Submissions Specialist - Clinical Trials (New South Wales)
🏢 Fortrea
📍 New South Wales

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