Precision for Medicine is seeking a Regulatory and Start Up Specialist to join our growing team in Hobart. You will manage regulatory submissions, prepare or support study start-up plans, and coordinate with CA/EC, ethics committees, and external sites to ensure timely activation of trials.
The ideal candidate has life sciences education and proven experience in regulatory or site start-up within CRO or pharma. English fluency, solid organization, and milestone tracking are essential to success.
📌 Site Activation (Hobart)
🏢 Precision for Medicine
📍 Hobart
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