Jennifer Keyser, MBA, is a seasoned and dynamic regulatory affairs professional with over 19 years of extensive experience in clinical research management. They served as a Clinical Trial Contracts Associate at the University of Kansas Medical Center, where they led study kick-off meetings and managed budget analyses. At Worldwide Clinical Trials, they directed study initiatives and maintained compliance with regulatory requirements as a Senior Specialist in Regulatory Affairs. Currently, as a Principal Regulatory Affairs Specialist at PPD, Jennifer provides regulatory expertise and strategic guidance for projects across multiple countries. They are pursuing a Bachelor's Degree in Psychology from the University of Missouri-Kansas City and hold an MBA in Health Care from Avila University.
Location
United States
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