Global Regulatory Strategy Lead for Drug Submissions

A leading pharmaceutical company in Santa Fe, New Mexico is seeking a Regulatory Affairs Specialist responsible for developing global regulatory strategies for investigational and marketed drugs. The ideal candidate should have a Bachelor's degree and significant experience in regulatory affairs, preferably within the pharmaceutical industry. Responsibilities include managing regulatory submissions and providing guidance to project teams. The role offers a competitive salary and comprehensive benefits including healthcare and 401(k) matching. #J-18808-Ljbffr