Precision Medicine Group, a leading life sciences CRO, is seeking a Regulatory and Site Start Up Specialist to drive regulatory submissions and site activation across assigned sites. The role requires coordination with CA/EC, IRB/EC submissions, and essential document management to ensure on-time activation.
The RSS will support budget reviews, translation coordination, and cross-functional collaboration with Feasibility, Clinical Operations, and Site Contracts teams to ensure regulatory
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📌 Global Regulatory & Site Start-Up Specialist (Sydney)
🏢 Precision Medicine Group
📍 Sydney
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