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Job ID88 Overview Responsible for the development, review, and submission of regulatory filings (e.g. Annual Reports, Supplements, CBEs (Changes Being Effected), Protocols, etc.), tracking and updating status reports, and supporting Regulatory Affairs senior management in all10/8/2015 Blue Ash, OH Save This Job
Job ID87 OverviewResponsible for independently developing regulatory strategy and filings (e.g. Annual Reports, Supplements, CBEs (Changes Being Effected), Protocols, etc.), providing critical review of CMC (Chemistry, Manufacturing, and Controls) and clinical submissions,10/8/2015 Blue Ash, OH Save This Job