Kissondra Morris, MS, MBA
Associate Director, PRC Lead
BMS
Kissondra Morris is the Oncology Protocol Review Committee Lead in the Clinical Center of Excellence at Bristol Myers Squibb, where she oversees the scientific rigor and quality of oncology clinical trial documents. With over 10 years of experience in drug development, she has held roles spanning Innovation and Digital Health, Study Optimization, and Trial Digitalization.
At BMS, she has partnered across functions and with external collaborators to introduce new approaches in RWD and trial innovation that improve study design, streamline site technology, and strengthen patient experience. Earlier in her career, she held research roles at Moffitt Cancer Center, the University of South Florida, and Intezyne. She holds an MBA, an MS in Biotechnology, a Graduate Certificate in Intellectual Property, and she has contributed over 4,000 volunteer hours in healthcare and environmental projects.