Ms. Ahmad is a versatile clinical professional with strong regulatory knowledge honed through extensive prior experience with planning, managing, and monitoring clinical trials, from initiation through close-out, both in the U.S. and overseas. Further, she is adept at building and managing trusted relationships with site teams, investigators, and sponsors. Ms. Ahmad has a natural talent for conducting peer training on various regulatory requirements and all aspects of clinical trial management. She leverages expert knowledge of clinical research protocols, data analysis methodologies, and clinical research processes to ensure that studies are conducted in compliance with SOP, ICH/GCP guidelines, study budgets, and industry best practices.
Ms. Ahmad received her Master of Science in Biotechnology from Georgetown University and her Bachelor of Science in Human Biology from Stanford University.
Ms. Ahmad has over 12 years of clinical research experience working on pharmaceutical and device studies
Ms. Ahmad is responsible for leading MCRA's Clinical Research Organization (CRO) operations, covering protocol development, study start-up planning, investigator identification, site qualification, monitoring, and clinical audits for US IDE and post-approval studies.