Global Regulatory Strategy & Submissions Lead

A leading pharmaceutical company is seeking a regulatory affairs professional in Little Rock, Arkansas. The role involves developing global regulatory strategies for investigational and marketed drugs, ensuring compliance with FDA submissions, and managing cross-functional teams. Candidates should have a Bachelor's degree and extensive experience in regulatory affairs, ideally with an RAC certification. This position offers a competitive salary range and comprehensive benefits, including healthcare coverage and a generous 401(k) match. #J-18808-Ljbffr