Mone’ Brown

Mone’ Brown has been with Clinical Research FastTrack since February 2021 and has over 12 years of Clinical Research experience. She has her Bachelors in Health Science and a Masters in Regulatory Science and Psychology from Johns Hopkins. She started her career in the industry as a Research Assistant in 2006 at a small clinic that specialized in Rheumatoid Arthritis before accepting a position with a Pharmaceutical company in 2012 as a Regulatory Document Specialist. Within her role at Amphastar Pharmaceuticals she performed duties from Study Start-Up to Close Out, creating Informed Consent and Assent forms, Phase 1 – Phase IV IRB Submissions as well as IND submissions, and NDA submissions to FDA, managed document control, edited study reports, and performed internal audit tasks. She has also worked as a Regulatory Specialist for Kaiser Permanente Research and the most recent Covance known now as Labcorp Drug Development. She has worked on a very wide range of therapeutic areas within her Clinical Research career.