PSI is seeking a clinical start-up qualified to drive site activation in Australia. You will coordinate between project teams and investigational sites, managing timelines, regulatory submissions, and TMF maintenance.
This hybrid role involves cross-functional collaboration and wearing multiple hats to ensure smooth startup execution. You will contribute to site budgets, contract negotiations, and regulatory document collection while coordinating with sites through the study lifecycle and
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📌 Hybrid Clinical Study Start-Up Specialist (Sydney)
🏢 Psicro
📍 Sydney
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