Novotech is seeking a Regulatory Start-Up Associate II to plan, prepare, and review ethics and regulatory authority submissions for clinical trials at country and site levels. The role requires coordinating start-up activities with RSM/PM and sites, ensuring adherence to ICH-GCP and local regulations.
The role is hybrid, based in Brisbane, Sydney or Melbourne, with 2 days in the office, and requires full unrestricted working rights. We offer flexible working options and development programs.
Global Regulatory Start-Up Associate II in Sydney employer: Novotech
Novotech is an exceptional employer that fosters a dynamic and collaborative work culture, perfect for those passionate about advancing their careers in toxicology and regulatory affairs. Located in Australia, we offer our employees comprehensive growth opportunities, competitive benefits, and the chance to work alongside industry experts on cutting-edge projects in clinical trials. Join us to make a meaningful impact in the field while enjoying a supportive environment that values innovation and professional development.
