Precision Medicine Group seeks a Regulatory and Site Start Up Specialist in Australia to manage regulatory submissions and site activation activities across assigned sites. You will prepare CTAs and dossiers for competent authorities and ethics committees, maintain essential documents, and collaborate with CRAs to ensure timely site activation.
You will support feasibility, budgeting, and guidance to in-country teams while staying compliant with local and international regulations.
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📌 Global Regulatory & Site Start-Up Expert (Sydney)
🏢 Precision Medicine Group
📍 Sydney
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