Julie Miller is Staff Vice President of Clinical Research for Carelon Research. In this role, Ms. Miller oversees our Clinical Research portfolio, including strategy, sales, operations, and leadership and provides functional expertise and innovative solutions for the execution of trials and studies. Her responsibilities include developing the Clinical Research business unit’s strategies, collaborating with investigators and clients on study design and concept development, setting team goals, and prioritizing strategic and process improvement initiatives. She also leads a comprehensive clinical research team, including project and program managers, remote and in-house clinical research associates, data managers, programmers, statisticians, and safety specialists.
Ms. Miller has over 25 years of research experience in the development and management of clinical research studies across therapeutic areas, including observational studies, registries, and Phase II to IV studies. Ms. Miller has a proven track record of operational leadership and innovation. She has extensive experience in administrative oversight, project management, and clinical operations, having served as a Data Coordinating Center Principal Investigator in several federally funded networks and grants, many in pediatric and underserved diseases, including the Pediatric Heart Network, BabyHug (Sickle Cell), the COVID MUSIC Study, and the Transfusion Medicine/Hemostasis Clinical Trials Network.
Ms. Miller also serves as a member of the National Heart, Lung, and Blood Institute (NHLBI)'s Clinical Trials Review Committee, has served on New England Research Institutes’ Institutional Review Board, and has contributed to many corporate policies and procedures.
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