CMC Regulatory Affairs Associate — Class III PMA Expert

A clinical research organization is seeking a regulatory affairs specialist responsible for managing submissions and government interactions for product approvals. The ideal candidate will have 3-5 years of experience, particularly with Class III implantable devices and related regulatory frameworks. Strong technical writing skills and a CMC background are essential for this role, which demands a creative approach to problem-solving and an advanced degree is preferred. #J-18808-Ljbffr