Southern Clinical Development Consulting is seeking a Senior Regulatory Affairs Specialist to lead regulatory strategy and submissions for sponsor products in Australia and New Zealand. You will own end-to-end dossiers, interact with the TGA and Medsafe, and manage multiple projects with sharp turnaround times.
Reporting to the Head of Regulatory Affairs, you will mentor juniors, contribute to templates and SOPs, and leverage modern tools including generative AI to improve quality and speed of
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Contact Details:
Southern Clinical Development Consulting Recruitment Team
