Lisa Parker, Ph.D.

Director, Center for Bioethics & Health Law
Dickie, McCamey & Chilcote Professor of Bioethics
Professor of Human Genetics, School of Public Health
Director, Master of Arts in Bioethics Program, University of Pittsburgh

Bio

Lisa Parker, a philosopher, is the Dickie, McCamey & Chilcote Professor of Bioethics, Director of the Center for Bioethics & Health Law, and Professor of Human Genetics in the School of Public Health. She directs the University’s Center for Bioethics & Health Law, as well as its interdisciplinary Master of Arts in Bioethics program in The Dietrich School of Arts and Sciences. She is a fellow of the Center for Philosophy of Science and a member of the Steering Committee in the Department of Gender, Sexuality, and Women's Studies, where she teaches courses on feminist theory and on gender and the body. She also teaches research ethics for the School of Public Health and the Institute for Clinical Research Education. With a national working group of the Association of Schools of Public Health, Dr. Parker edited Ethics and Public Health: Model Curriculum (Association of Schools of Public Health, 2003), and she is an Associate Editor of the forthcoming Handbook of Public Health Ethics (Oxford University Press). She is a co-investigator for an international research ethics training program sponsored by the Fogarty International Center of the NIH focused on China, and has provided research ethics training in Kolkata and New Delhi, India, as well as Egypt, through three other Fogarty-sponsored training programs. Dr. Parker has published extensively on ethical concerns related to the design and conduct of research, particularly genetic research and mental health research, as well as on aesthetic surgery, confidentiality, and informed consent. She has sustained interest in employing feminist approaches to bioethical issues and in the critical analysis of bioethics as a social practice. Much of her work examines the effect of new technologies and policies on health disparities and on those situated with less power in social hierarchies.

Dr. Parker collaborates with investigators across the University, as well as nationally and internationally, on both empirical studies and theoretical and policy analyses. With colleagues in the CEP, she offered guidance regarding discovery and management of incidental findings in the use of DNA to identify human remains following natural disasters and armed conflict. With colleagues in the Department of Psychiatry, Dr. Parker was involved in a community-based project to investigate the care of elderly living with depression and other severe mood disorders. She serves as a co-investigator and ethics consultant on studies involving biobanking and whole exome/genome sequencing in different patient populations. With colleagues in India, she is investigating differing conceptions of privacy and analyzing the appropriateness of privacy protection requirements utilized in the US and by the NIH when applied in Indian research and patient care contexts.

Dr. Parker’s recent research has focused on the ethical management of incidental findings and return of research results, privacy protection, pharmacogenomic research and genomic medicine. She chaired the Genomics and Society Working Group of the National Advisory Council for Human Genome Research for the NHGRI and served on two NIH Working Groups — Managing Incidental Findings in Human Subjects Research and Managing Incidental Findings and Research Results in Genomic Biobanks & Archives. She serves on the Expert Scientific Panel of the Electronic Medical Records and Genomics (eMERGE) Network and provides ethics expertise to the University of Pittsburgh’s Institute for Personalized Medicine.