UNC Research Ethics Grand Rounds

All of Us

Developing a Scalable Consent for Diverse Participant Engagement

        The All of Us Research Program, a keystone of the Precision Medicine Initiative, aims to assemble … Continued

Burgoo vs. Quinoa

Reconciling Local vs. Global Governance in Networked Biorepositories

As biomedical research generates ever-growing requirements for large sample sizes, it has increasingly depended on biorepositories to provide biosamples and … Continued

Pathways to Trust

Genomics, Precision Medicine, and Health Disparities

Wylie Burke, MD, PhD is Professor and former Chair of the Department of Bioethics and Humanities at the University of … Continued

Digital Informed Consent for Pragmatic and Other Large-scale Trials

Digital technologies are changing how people are recruited to research and raising new ethical, practical, and social considerations. Informed consent … Continued

Updating Regulations for Human Subjects Research

The New Common Rule has Arrived! What Changes are Coming?

In early 2017, just prior to the change in administration, the 18 federal agencies that share the “Common Rule” that … Continued

Reflecting on “Experimenting with Humans and Animals”

Looking at human and animal experimentation together revealed intersections and differences that were not immediately evident. This talk will look at … Continued

Ethical and Regulatory issues in “E-consent” to Clinical Research

As translational researchers turn to electronic information sources for clinical research recruitment, they are increasingly using on-line communication tools to … Continued

Ethics of treatment interruption in HIV cure trials

Normative and empirical perspectives

Gail E. Henderson, PhD, is professor of Social Medicine in the School of Medicine, and Director of the UNC Center … Continued

Duties to look, return, or rescue

Moral obligations and incidental findings in research

Dr. Karen Meagher graduated in Hamilton College in 2004 with a B.A.in biology. She received a PhD in Philosophy from … Continued

Employees as research participants

Ethical and regulatory considerations

Dr. Resnik has an M.A. and Ph.D. in philosophy from the University of North Carolina at Chapel Hill and J.D. … Continued

Should we take the moral concerns of biobank donors seriously?

Biobanking is becoming an increasingly important component of genomic and medical research. President Obama’s Precision Medicine Initiative ― which proposes the … Continued

Join the Conquest

Increasing participation in clinical research in North Carolina

Clinical trial recruitment is in crisis. The public typically encounters clinical trial information in controversies or study-specific recruitment ads, which … Continued

Patient perspectives on research on standard medical practices

Implications for consent

Dr. Kevin P. Weinfurt is Professor of Psychiatry and Behavioral Sciences, and Professor of Psychology and Neuroscience at Duke Clinical … Continued

Informed consent for oncology phase 1 clinical trials in the 21st century

Dr. Katie Reeder-Hayes and Dr. Claire Dees, UNC Division of Oncology, Lineberger Comprehensive Cancer Center.

Automatic placement of genomic research results in medical records

Do researchers have a duty? Should participants have a choice?

In genomics research, it is becoming common practice to return individualized primary and incidental findings to participants and several ongoing major … Continued

Proposed changes to the Common Rule IRB regulations

Step 2 in changing the world as we know it

On September 2, 2015, the U.S. Department of Health and Human Services announced its long-awaited proposal to revise the “Common … Continued

Handling research animal ethics

Interactions between science and welfare

Research on animal welfare is organized around a distinction between the care of animals and their use in experiments. Nicole … Continued

Rules, rebels and scientific integrity

Do you have to be a “good scientist” to be a good scientist?

Most courses and texts on the responsible conduct of research imply that the professional ethical norms they teach also facilitate … Continued

The ethics of clinical research during an epidemic

Lessons from Ebola

The 2014 Ebola epidemic in west Africa is the most severe and largest documented to date. It is also the … Continued

Paying research “volunteers”

Ethical and regulatory concerns

Compensating research participants has been the subject of national debate for some time. In this presentation, I will review the … Continued

Dignitary and other intangible harms in clinical research

Regulatory and ethical challenges

Can research subjects be “wronged” even if not physically injured in a clinical trial? Thorny questions of how to account … Continued