Senior Global Start-Up Regulatory Specialist

A full-service clinical contract research organization is looking for a Senior Regulatory Affairs study Start Up Specialist in Covington, KY. This role involves managing regulatory documentation submissions to various authorities, ensuring compliance with requirements, and maintaining documentation quality. Candidates should have at least 5 years of regulatory experience in the pharmaceutical industry and an associate's or bachelor’s degree in a health-related field. The position offers opportunities for career advancement and a supportive working environment. #J-18808-Ljbffr