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You'll be the primary regulatory CMC voice on cross-functional matrix teams, covering everything from early clinical trial applications through to new marketing authorizations, post-approval changes, and full lifecycle management. That means you won't
A key focus area of the position is the preparation of regulatory CMC documentation for small molecule products during development and commercial stage, in a manner that is scientifically sound, commercially viable and in accordance with current
In this role, you will lead the development and execution of global clinical-regulatory strategies for Novocure’s Class IIb/III medical device portfolio, supporting programs from early clinical development through commercialization and lifecycle