12 Oct
|
Novotech
|
Sydney
Novotech is seeking a Regulatory Start-Up Associate II to plan, prepare and review country- and site-level regulatory submissions during the start-up phase of clinical trials, ensuring compliance with ICH-GCP and local regulations.
You will work with the Regulatory Start Up Manager and project team, manage submission timelines, coordinate with ethics committees and regulatory authorities, and deliver quality start-up deliverables with minimal supervision.
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📌 Regulatory Start-Up Associate II: Lead Country Submissions (Sydney)
🏢 Novotech
📍 Sydney