Novotech is seeking a Regulatory Start-Up Associate II to plan, prepare, and review country- and site-level ethics and regulatory submissions during the start-up phase of clinical trials. The role ensures compliance with ICH-GCP and local regulations while coordinating with the Regulatory Start Up Manager (RSM), Project Manager, and sites to drive timely approvals.
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You will manage submission deadlines, provide local regulatory insights, and uphold submission timelines across country and site