This pharmaceutical company is committed to developing and commercializing innovative therapeutics to improve the lives of patients with serious retinal diseases. They are seeking a Vice President of Regulatory Affairs to provide team leadership and strategic input for their product portfolio. Reporting into the Chief Regulatory & Quality Officer, the Vice President will be responsible for overseeing overall regulatory strategy in close collaboration with Reg CMC and Regulatory Operations functions, managing compounds through development for regulatory approval, as well as life cycle management of marketed products. This individual will oversee an upcoming NDA submission, focusing on managing non-clinical, clinical, label/labeling development and maintenance, and overseeing Medical Legal Regulatory Review Committee of Advertising Promotional Review process, and work closely with Health Authorities. This company offers robust total rewards in a science-based entrepreneurial cultur...