Precision for Medicine in Australia seeks a Regulatory Start-Up Specialist to lead site activation and regulatory submissions. You will prepare and submit Clinical Trial Applications, liaise with authorities, and ensure timelines and compliance.
You will work with local IRB/Ethics committees, site contracts, budgets, and cross-functional teams to secure timely activations and study approvals, while maintaining TMF readiness and process improvements.
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📌 Site Activation & Regulatory Start-Up Specialist (Australia)
🏢 PFM
📍 Australia
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