Global CMC Regulatory Consultant (Senior)

A leading global clinical research organization is seeking an experienced CMC Regulatory Affairs Senior/Consultant to join their team in Boston. The role involves providing regulatory strategy input, preparing documentation for various regulatory submissions, and collaborating with cross-functional teams to ensure compliance and enable timely product approvals. Ideal candidates have extensive CMC regulatory experience, strong problem-solving skills, and the ability to manage multiple projects in a global environment. #J-18808-Ljbffr