Global Regulatory Strategy & Submissions Lead

A pharmaceutical company in Salt Lake City seeks a Regulatory Affairs Specialist to develop and manage global regulatory strategies for prescription drugs. The ideal candidate will have a Bachelor's degree and 5+ years of experience in regulatory affairs, preferably with FDA interactions. Responsibilities include preparing regulatory submissions, providing guidance in project team meetings, and collaborating with cross-functional teams. This position offers a comprehensive benefits package and an attractive compensation range. #J-18808-Ljbffr