Global CMC Regulatory Affairs Lead

A biotechnology firm is seeking an Associate Director, Regulatory Affairs CMC, to develop regulatory strategies for drug development. The role involves supporting regulatory submissions and ensuring compliance with health authority requirements. Ideal candidates should have a strong background in clinical research, a minimum of 8 years’ experience, and excellent knowledge of CMC regulations. This position is based in Boston, MA, and offers a competitive salary package with potential for remote work. #J-18808-Ljbffr