Hybrid CMC Regulatory Affairs Consultant | Global Submissions

A recruitment consultancy is seeking a Regulatory Affairs Consultant in Cambridge, Massachusetts. This strategic role focuses on providing regulatory CMC expertise for global pharmaceutical development. Responsibilities include preparing regulatory submissions and coordinating with health authorities. Candidates should have 3-5 years in the pharmaceutical industry, preferably in regulatory roles. This position offers a hybrid work model and fosters collaboration across locations, aiming for efficient submission processes and stakeholder coordination. #J-18808-Ljbffr