Regulatory CMC Writer & Project Manager (Contract)

A global workforce management provider is seeking an experienced CMC Writer in Paramus, NJ to support regulatory submissions. This temporary role requires strong technical writing and project management skills, focusing on high-quality documentation for health authorities. Candidates should have at least 5 years in pharmaceutical regulatory writing, a relevant degree, and proficiency in Microsoft Office. Additional experience with IND/NDA/BLA submissions is preferred. The work involves ensuring compliance with regulations and managing project timelines. #J-18808-Ljbffr