06 Sep
|
Fortrea
|
Sydney
Fortrea is seeking a regulatory submissions specialist to act as the primary liaison with investigative sites. You will collect and compile essential documents, ensure timely IRB/IEC and authority submissions, and coordinate with internal teams and vendors to maintain project timelines.
The role requires knowledge of ICH/GCP, regulatory guidelines, and a proactive approach to risk escalation, with a focus on audit readiness and quality review.
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📌 Clinical Trials Start-Up Specialist (Sydney)
🏢 Fortrea
📍 Sydney