Pharmacovigilance & Regulatory Affairs Associate

A leading pharmaceuticals company in Columbia, SC is seeking a qualified professional to manage adverse event reports and regulatory documentation. The role requires a relevant scientific degree, ideally PharmD or RN, with at least 2 years of experience in Drug Safety and Regulatory Affairs. Responsibilities include evaluating and processing reports, communicating with regulatory authorities, and ensuring compliance with regulations. This offers a competitive salary based on experience and requires excellent analytical and communication skills. #J-18808-Ljbffr