Speaker Profile
Clarence Buddy Creech Ii

Clarence Buddy Creech Ii MD, MPH

Pediatrics, Pediatric Emergency Medicine, Pediatric Infectious Disease
Nashville, Tennessee, United States of America

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Dr. Clarence Buddy Creech II graduated cum laude from Vanderbilt University before attending the University of Tennessee College of Medicine. After graduating with high honors, he joined the pediatric housestaff at Monroe Carell Jr. Children's Hospital at Vanderbilt and was Chief Resident in Pediatrics in 2002. During his pediatric infectious diseases fellowship at Monroe Carell, Dr. Creech completed the Master's in Public Health degree and became part of the Vanderbilt Clinical Research Scholars (VCRS) Program, a competitive NIH K12 award given to young investigators at VUMC. He joined the faculty in July 2006 as Assistant Professor of Pediatric Infectious Diseases and now serves as Director of the Vaccine Research Program and Program Director of the Pediatric Infectious Diseases Fellowship.

Dr. Creech serves as Director of the VVRP, Principal Investigator of the NIH-funded Vaccine and Treatment Evaluation Unit (VTEU), and Co-Principal Investigator of the CDC-funded Clinical Immunization Safety Assessment (CISA) Project. His research focuses primarily on the clinical and molecular epidemiology of S. aureus infections and on the immune response to vaccination and disease. He has served as PI for numerous studies, including a Phase I adenovirus-vectored malaria vaccine study, studies of inactivated and live-attenuated influenza vaccines in children, comparative effectiveness studies of skin/soft tissue infections and pneumonia, and studies of vaccines targeting pertussis and Staphylococcus. In 2007, he was the recipient of the IDSA/SHEA Young Investigator Award in MRSA, and in 2012, he received the PIDS Young Investigator Award.

He is currently leading studies to determine the optimal duration of therapy for children with pneumonia; to define the immune response to influenza vaccination using a systems vaccinology approach; to define the immune response to S. aureus infections in children and adults; and to compare whole-cell pertussis and acellular pertussis vaccines in children, using ribosome profiling as a transcriptomics tool.1093742033

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