Chiamaka D. is a Senior Clinical Research Associate at Esperion, with a proven track record of enhancing vendor utilization and site compliance in clinical studies. Prior experience includes roles at Covance, where Chiamaka conducted site evaluations and streamlined study initiation processes, and at Medpace, where oversight of multiple clinical trials and training for proper reporting of adverse events were key responsibilities. Chiamaka began in clinical research as a Clinical Research Coordinator at UC Davis Health, achieving significant improvements in patient recruitment and compliance. Chiamaka holds a degree in Public Health from the University of Houston.
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