Precision Medicine Group in Melbourne is seeking a Regulatory and Start Up Specialist to manage Clinical Trial Application Forms and submissions.
This role involves collaboration with Competent Authorities and Ethics Committees, maintaining project trackers, and ensuring compliance with regulations.
Candidates should have a Bachelor's in life sciences, 1+ years in regulatory roles, and solid communication skills.
This is an chance to work in a agile environment focused on advancing precision medicine.
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📌 Site Activation & Regulatory Specialist Melbourne
🏢 Precision Medicine Group
📍 Melbourne
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