CMC Regulatory Affairs Associate II — Dossier Lead

A leading Contract Research Organization in Baltimore, MD is seeking a skilled professional to manage and compile CMC sections of marketed product variations. The ideal candidate should have experience in pharmaceutical project management, regulatory submissions, and strong communication skills. Responsibilities include collaborating with teams to ensure accuracy in CMC dossiers and facilitating project meetings. This position requires a Bachelor's degree in science and at least 5 years of relevant experience. Competitive salary and benefits offered. #J-18808-Ljbffr