CTI in Sydney, Australia seeks a Regulatory Affairs Study Start Up Specialist II to support regulatory activities for clinical studies in multiple countries. The role requires coordinating submissions, document quality checks, and collaboration with sponsors and site teams across regions.
You will ensure compliance with ICH/GCP and country regulations, adapt study documents, and manage regulatory timelines.
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📌 Regulatory Start Up Expert – Hybrid Sydney (Australia)
🏢 Consulting
📍 Australia
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