Precision for Medicine seeks a Regulatory and Site Start Up Specialist to lead regulatory activities for clinical trials.
You will manage initial and follow-up submissions to Competent Authorities and IRBs, review informed consent forms, and support site contracts and budget negotiations.
Solid regulatory knowledge and site start-up experience are essential.
The role involves coordinating with cross-functional teams to ensure on-time site activation, maintaining essential documents, and
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📌 Regulatory & Site Activation Expert (Sydney)
🏢 Precision for Medicine
📍 Sydney
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