Sumedha Chawla completed her medical training at Era’s Lucknow Medical College, India and earned her Master of Public Health at The University of Texas Health Science Center, Houston. As a clinical research professional, Sumedha has over 5 years of experience managing and coordinating industry-sponsored and investigator-initiated clinical trials. In this position, Sumedha collaborates with the section staff to plan, prepare, implement, and monitor clinical research activities, and provide assistance in the writing, preparation, and submission of material to the Institutional Review Board (IRB) and the Food and Drug Administration (FDA).