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.You will manage submission deadlines, provide local regulatory insights, and uphold submission timelines across country and site
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