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Associate Director, Regulatory Affairs CMC Boston United States,  


Posted on : 29 March 2017

Project Description

OBJECTIVES:Develops and leads the execution of regulatory CMC development and registration strategies as the RA CMC member on Regulatory, Pharmaceutical Development, and Production project teams for assigned products throughout clinical development and commercial lifecycle with minimal supervisionDevelops and applies a comprehensive understanding of global RA CMC regulations and guidelines to projects

Locations

Boston Massachusetts United States

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