Cassie Newell has over 23 years of experience and specializes in authoring clinical study reports, and Investigator Brochures. Mrs. Newell has experience in leading global clinical, operational management teams/programs (I-IV), clinical project and study management, planning and implementing standard processes, partnership programs, and portfolio management. Mrs. Newell specializes in providing recommendations for site selection and managing clinical trials, which includes monitoring, data management, medical writing; all while overseeing timelines, budgets, and staff. Her therapeutic area experience includes; mental/cognitive disorders, neurology, pediatrics, respiratory, rare disease, cardiovascular, endocrine/metabolic and gastrointestinal.
Education