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 I – 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. In her personal time, Mone’ enjoys spending time with her family, as well as being very adventurous and riding extreme Rollercoasters, skydiving, traveling, singing, and mentoring those who want to enter into Clinical Research. Mone’ has a passion for Clinical Research and truly loves knowing that she’s making a difference and impacting so many lives.