Senior Regulatory CMC Lead for Global Drug Development

A leading pharmaceutical company is seeking an Associate Director in Regulatory CMC. This role involves contributing to global regulatory strategies, managing submission processes for clinical trials and marketing applications, and ensuring compliance with regulatory standards. Candidates should have over 8 years of experience in CMC regulatory affairs, with a focus on small molecule drug development. This position offers a competitive salary and a hybrid work model based in California or New Jersey. #J-18808-Ljbffr