Regulatory Affairs CMC Strategy Lead — Principal Consultant

Opus-Regulatory in Miami is seeking a Principal Consultant in Regulatory Affairs CMC to oversee regulatory submissions and client relationships. The role requires at least 7 years in the pharmaceutical/biotech industry and 5 years in regulatory affairs CMC. Responsibilities include managing submissions, providing regulatory guidance, and interacting with authorities. Comprehensive benefits include medical, dental, 401(k), and PTO, fostering a supportive work environment. #J-18808-Ljbffr