Parexel is seeking a Clinical Trial Site Activation Specialist to drive site activation and regulatory submissions across Australia. You will coordinate IIP preparation, IRB submissions, and communications with ethics committees while ensuring timely project milestones.
The role requires 2+ years in clinical site management, strong GCP knowledge, and ability to work across multiple sites. Travel may be required in a global setting.
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📌 Remote Clinical Site Activation Specialist (Australia)
🏢 Parexel
📍 Australia
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