Site Activation & Regulatory Specialist

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 strong communication skills. This is an opportunity to work in a dynamic environment focused on advancing precision medicine. #J-18808-Ljbffr