Associate Director of Regulatory Affairs The Associate Director of Regulatory Affairs for this Northeastern company will be responsible for assuring that documents are prepared in a sound, clear and timely manner and are consistent with FDA regulatory requirements. The Associate Director will provide regulatory guidance and scientific support for all submissions. The ideal candidate for this position would have at least eight years experience in the pharmaceutical industry with a track record of success in regulatory affairs. A background in CNS is helpful. Experience with original IND/NDAs, amendment and supplement filings is essential. [ back ]
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