Director, Regulatory Affairs The Director of Regulatory Affairs for a Northeastern start-up company will be responsible for overseeing all aspects of Regulatory submissions, particularly CMC sections. This position requires a thorough understanding of the regulatory process and FDA requirements as they pertain to the preparation and submissions of the CMC sections of INDs, NDAs, and ANDAs. The successful candidate will have a strong track record in the pharmaceutical industry with demonstrated success in regulatory submissions. [ back ]
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