CTI Clinical Trial and Consulting Services in Sydney, NSW is seeking a Regulatory Affairs Study Start Up Specialist II for a hybrid work arrangement. You will coordinate regulatory submissions, ensure country-specific compliance, and liaise with sites and sponsors to maintain filing accuracy across multiple regions.
Ideal candidates will have 3–5 years of regulatory experience in pharma/CRO settings, strong English communication, and a detail-oriented, collaborative approach to support
Senior Regulatory Start-Up Specialist Clinical Trials in Sydney employer: CTI Clinical Trial and Consulting Services
CTI is an exceptional employer for the Regulatory Affairs Study Start Up Specialist II role, offering a dynamic work culture that prioritises collaboration and continuous learning. Located in Australia, employees benefit from a supportive environment that encourages professional growth through ongoing training and development opportunities, while also enjoying the satisfaction of contributing to impactful clinical studies that enhance healthcare outcomes.
Contact Details:
CTI Clinical Trial and Consulting Services Recruitment Team
