A conversation with Dr. Greg Campbell.
A conversation with Dr. Greg Campbell.
复制标题
与格雷格·坎贝尔博士的对话。
DOI:
10.1080/10543406.2016.1226331
复制
发表时间:
2016
影响因子:
1.1
通讯作者:
Yue,LillyQ
中科院分区:
文献类型:
--
作者:
Liu,Aiyi;Yue,LillyQ
Dr. Gregory Campbell received his PhD in Mathematical Statistics from the Florida State University in 1976. After his completion of graduate studies, Dr. Campbell took a faculty position as an assistant professor in the Department of Statistics at Purdue University, and later joined the intramural program of the National Institutes of Health, where he was promoted to a senior investigator with tenure, and he served as the Acting Chief for the Laboratory of Statistical and Mathematical Methodology, and then Chief of the Analytical Biometrics Section. Dr. Campbell joined the Food and Drug Administration (FDA) in 1995, and served as the Director of the Division of Biostatistics in the Office of Surveillance and Biometrics of the Center for Devices and Radiological Health (CDRH) at the FDA until his retirement from the federal government at the end of June 2015. His extraordinary leadership has resulted in the growth of the Division from 18 mathematical statisticians to 62 in five branches. He has made exceptional contributions to public health, the FDA, and medical device industry by leading the Division to provide statistical support to CDRH as a whole and, in particular, the statistical reviews of FDA’s pre-market device submissions, bringing in numerous important and innovative medical devices to the market place.During his nearly 33 years of federal service, Dr. Campbell has sustained high levels of professionalism and dedication. Because of his distinguished contributions as a driving force and a great leader in statistical innovations in the medical device world, the course of medical device evaluation and regulatory science has been greatly shaped. His pioneer work and sustained efforts in adapting and advancing the implementation in a regulatory environment of Bayesian statistics, causal inference, adaptive design, missing data, and diagnostic test methodology have made phenomenal, far reaching, and long-lasting impacts to public health and resulted in the increase of the integrity of clinical study design and the creditability of study results as well as the consistency, transparency, effectiveness, and predictability of regulatory decision-making for the FDA and industry. Dr. Campbell has been recognized as an internationally renowned statistical leader in regulatory science. Dr. Campbell served in leadership positions for the Eastern North American Region (ENAR) of the International Biometric Society, the Society for Clinical Trials, and the FDA Statistical Association (FDASA). He played a distinguished leadership role in the establishment of the statistical community of medical devices and diagnostics, and was instrumental in the formation of the American Statistical Association (ASA)’s Section on Medical Devices and Diagnostics (MDD). Dr. Campbell was a member for over 10 years of the prestigious Senior Biomedical Research Service (SBRS) in the Department of Health and Human Services, and also served for 15 years on the SBRS credentialing committee. He has been a Fellow of the American Statistical Association since