Travere Therapeutics in San Diego seeks an Associate Director, Labeling Strategy to lead global regulatory labeling across the product lifecycle. You will develop, negotiate, implement and maintain labeling content including USPI, CCDS, and TPL, collaborating with Regulatory, Clinical Development, Medical Affairs and Legal. This role requires 8+ years in pharma/biotech, strong leadership, and a track record in global labeling strategy, with readiness to travel up to 10% domestically and

Also on the board Same function, level within a rung

Level

Manager

Location

Kansas City, MO

Occupation

Regulatory Affairs Managers

Industry

Biological Product (except Diagnostic) Manufacturing

Posted

yesterday

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