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Trained in medical physiology, Nelson previously held
faculty appointments at the Mayo Clinic, with a fellowship conducting
human studies in Europe; and the University of Rochester, where he was
director of research in a clinical gastroenterology unit and chair of
a hospital Institutional Review Board (IRB). His move to UNC-Chapel Hill
in 1998 represented a fulltime commitment to research ethics, and he now
has global oversight responsibility for 8 IRBs and approximately 4000
research studies.
A national leader in the field of human research protections, Nelson
is past-president of the Applied Research Ethics National Association
(ARENA), consultant to the federal Office for Human Research Protections
(OHRP), council member of the Association for the Accreditation of Human
Research Protection Programs (AAHRPP), founding member of the Council
for Certification of IRB Professionals (CCIP), and served as a liaison
to the National Bioethics Advisory Commission (NBAC). He was recently
appointed co-chair of a federal subcommittee of the Secretary’s
Advisory Committee on Human Research Protection (SACHRP, DHHS), charged
to review and make recommendations on the regulations that govern this
area. Nelson is also a co-investigator on several NIH grants on issues
surrounding research ethics, and frequently lectures on related topics. Selected publications: Lynn MR, Nelson DK. (2005) Common (mis)perceptions about IRB review of human subjects research. Nurs Sci Q. 18:264-70. King NM, Henderson GE, Churchill LR, Davis AM, Hull SC, Nelson DK, Parham-Vetter PC, Rothschild BB, Easter MM, Wilfond BS. (2005) Consent forms and the therapeutic misconception: the example of gene transfer research. IRB. 27:1-8. Henderson GE, Davis AM, King NMP, Easter ME, Zimmer CR, Rothschild BB, Wilfond BS, Nelson DK, Churchill LR. (2004) Uncertain benefit: investigators' views and communications in early phase gene transfer trials. Mol Ther 10:225-231. Churchill LR, Nelson DK, Henderson GE, King, NMP, Davis AM, Leahey E, Wilfond BS. (2003) Assessing benefits in clinical research: why diversity in benefit assessment can be risky. IRB 25:1-8. Califf RM, Morse MA, Wittes J, Goodman SN, Nelson DK, DeMets D, Iafrate RP and Sugarman J. (2003) Toward protecting the safety of participants in clinical trials. Control Clin Trials 24:256-271. |
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contact information: [phone] [email] |
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