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.
Site Activation & Regulatory Specialist in Melbourne employer: Precision Medicine Group
At Precision for Medicine, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our commitment to employee growth is evident through ongoing training and development opportunities, particularly in the dynamic fields of Oncology and Rare Disease. Located in a vibrant area, we offer a supportive environment where team members can thrive while making a meaningful impact on the future of life sciences.
