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Faculty List
Faculty By Last Name
A | B | C | F | G | H | J | K | L | M | O | P | R | S | W
Emily E. Anderson, PhD, MPH
Project Director, Illinois Prevention Research Center
Institute for Health Research and Policy
University of Illinois at Chicago
Chicago, IL
eander6@uic.edu
Speaker - Session: C1: Basic: “Informed Consent in Research”
Tom Aufderheide, MD
Professor of Medicine
Associate Chair of Research Affairs
Medical College of Wisconsin
Milwaukee, WI
taufderh@mcw.edu
Speaker - Session: C4: Hot/Important: “Emergency Research without Informed Consent”
Lisa Barnes, PhD
Associate Professor, Rush Alzheimer's Disease Center
Rush University Medical Center
Chicago, IL
lisa_l_barnes@rush.edu
Moderator - Plenary Session A: “Research with Minority Populations”
Judith Blacklidge, MS
Director, Research Compliance and Safety
Loyola University Medical Center
Maywood, IL
jblacklidge@lumc.edu
Moderator - Breakout Session A1: Basic “Historical Overview”
Elizabeth Buchanan, PhD
Director, Center for Information Policy Research
School of Information Studies
University of Wisconsin
Milwaukee, WI
eliz1679@uwm.edu
Speaker - Session: A2: Socio-Behavioral: “Research Ethics 2.0: Internet Research Ethics and the IRB”
Philip M. Budashewitz, BS Pharm, MA
Captain U.S. Public Health Service
Associate Director, Clinical Research Policy Analysis and Coordination Program (Crpac)
National Institutes of Health (NIH)
Rockville, MD
budashewitzp@od.nih.gov
Speaker - Panel: “What's New and Important from the Feds?”
David Clark, PhD
Assistant Dean for Clinical Research
Professor of Psychiatry
Medical College of Wisconsin
Milwaukee, WI
dclark@mcw.edu
Moderator - Breakout Session C4: “Emergency Research without Informed Consent”
Ellen Wright Clayton, MD, JD
Rosalind E. Franklin Professor of Genetics and Health Policy
Director, Center for Biomedical Ethics and Society
Professor of Pediatric; Professor of Law
Vanderbilt University
Nashville, TN
ellen.clayton@vanderbilt.edu
Moderator - Session B4: Hot/Important Topic: “Data Owed to Research Subjects”
Jordan Cohen, MD
Professor of Medicine
George Washington University School of Medicine
Washington, DC
msdjjc@gwumc.edu
Speaker - Plenary Session B: “Managing Financial Conflicts of Interest in Human Subjects Research”
Jeffrey Cooper, MD
Director
Huron Consulting
Chicago, IL
jcooper@huronconsultinggroup.com
Speaker - Session C2: Social-Behavioral: “Data Security and Mobile Devices: What Should Institutional Policy Say about Laptops and Other Devices That Move Between Your Office and Home”
Michelle Feige, MSW
Public Health Analyst
Office for Human Research Protections (OHRP)
Rockville, MD
Michelle.Feige@hhs.gov
Speaker - Session B1: Basic: “Human Subjects Protections”
Draco DuShea Forte, MEd
Manager
Sonnenschein Health Care Group
Chicago, IL
dforte@sonnenschein.com
Moderator - Session B1: Basic: “Human Subjects Protections”
Norman Fost, MD, MPH
University of Wisconsin, Madison
Professor, Pediatrics and Medical History and Bioethics
Director, Program in Bioethics, Department of Pediatrics
University of Wisconsin Hospital
Milwaukee, WI
ncfost@wisc.edu
Speaker - Session C4: Hot/Important: “Emergency Research without Informed Consent”
Stephanie Malia Fullerton, DPhil
Assistant Professor
Department of Bioethics and Humanities
University of Washington School of Medicine
Seattle, WA
smfllrtn@u.washington.edu
Speaker - Session B4: Hot/Important Topic: “Data Owed to Research Subjects”
Jorge O. Galante, MD, DMedSci
Professor of Orthopedic Surgery
The Granger Director of the Rush Arthritis and Orthopedics Institute
Rush Arthritis and Orthopedics Institute
Chicago, IL
jgalante@aol.com
Speaker - Plenary Session B: “Managing Financial Conflicts of Interest in Human Subjects Research”
Kate L. Gottfried, JD, MSPH
Senior Director, Research Integrity and Regulatory Affairs
Rush University Medical Center
Chicago, IL
Kate_l_Gottfried@rush.edu
Moderator - Breakout Session C1: Basic: “Managing Financial Conflicts of Interest in Human Subjects Research”
Phil Greenland, MD, NU
Harry W. Dingman Professor of Preventive Medicine and Medicine
Sr. Associate Dean for Clinical and Translational Research, Director, Northwestern University Clinical and Translational Sciences Institute
Northwestern University
Chicago, IL
p-greenland@northwestern.edu
Speaker - Session A4: Hot: Translational Research: “How it’s done in Chicago: Efforts to Reduce Regulatory Barriers for Translational and Clinical Research”
Deborah A. Gross, DNSc, RN, FAAN
Professor, Leonard and Helen Stulman Endowed Chair in Mental Health and Psychiatric Nursing
Johns Hopkins School of Nursing
Johns Hopkins School of Medicine
Department of Psychiatry and Behavioral Sciences
Baltimore, MD
dgross17@son.jhmi.edu
Speaker - Session B2: Socio-Behavioral: “Engaging the Hard to Engage”
Stephanie C. Guzik, RN, BSN, MBA
Assistant Director, Research Integrity and Regulatory Affairs
Rush University Medical Center
Chicago, IL
Stephanie_Guzik@rush.edu
Moderator - Breakout Session C1: Basic:“Informed Consent in Research”
Stuart Horowitz
Managing Director
Huron Consulting
Chicago, IL
shorowitz@huronconsultinggroup.com
Speaker - Session C2: Social-Behavioral: “Data Security and Mobile Devices: What Should Institutional Policy Say about Laptops and Other Devices That Move Between Your Office and Home”
Kathy Hudson, PhD (invited)
Chief of Staff
Office of the Director
National Institutes of Health
U.S. Department of Health and Human Services
Bethesda, MD
Kathy.Hudson@nih.gov
Keynote Speaker: "Directing Research in the Early 21st Century"
Bryan James, PhD
Instructor, Post-doctoral fellow, Rush Alzheimer’s Disease Center
Rush University Medical Center
Chicago, IL
Bryan_James@rsh.net
Speaker - Session C3: Advanced Topic: Special Populations ("Informed Consent along the Cognitive Spectrum: Research Issues in Mild Cognitive Impairment and Dementia")
Steven Jones, PhD
Professor, Department of Communication
University of Illinois at Chicago
Chicago, IL
sjones@uic.edu
Speaker - Session A2: Socio-Behavioral: “Research Ethics 2.0: Internet Research Ethics and the IRB”
David Kaufman, PhD
Director of Research and Statistics
Genetics and Public Policy Center
Johns Hopkins University
Washington, DC
dkaufma2@uic.edu
Speaker - Session B4: Hot/Important Topic: “Data Owed to Research Subjects”
Romina Kee, MD, MPH
Clinical Investigator
Collaborative Research Unit (CRU)
Department of Medicine
Cook County Health & Hospitals Systems
Chicago, IL
rkee@cchil.org
Speaker - Plenary Session A: “Research with Minority Populations”
Rick Kittles, PhD
Associate Professor, Department of Medicine, Section of Genetic Medicine
The University of Chicago
Chicago, IL
rkittles@medicine.bsd.uchicago.edu
Speaker - Plenary Session A: “Research with Minority Populations”
Charles W. Lidz, PhD
Research Professor, Department of Psychiatry; Medical School
University of Massachusetts
Worcester, MA
Charles.Lidz@umassmed.edu
Speaker - Session A3: Advanced: “Providing Clinical Care in Clinical Trials: Ethical Dilemmas and Resolutions”
Rebecca Ann Lind, PhD
Assistant Vice Chancellor for Research
Associate Professor of Communication
University of Illinois at Chicago
Chicago, IL
rebecca@uic.edu
Moderator - Breakout Session: A2 “Behavioral Research Ethics 2.0: Internet Research Ethics and the IRB”
Bret Moberg, JD, LLM
Rosalind Franklin University of Medicine and Science
Chief Compliance Counsel and Assistant Professor
North Chicago, IL
bret.moberg@rosalindfranklin.edu
Speaker - Session A1: Basic: “Historical Overview”
James L. Mulshine, MD
Associate Provost for Research
Rush University Medical Center
Chicago, IL
James_Mulshine@rush.edu
Moderator - Breakout Session A4: Hot/Translational Research: “How it’s Done in Chicago: Efforts to Reduce Regulatory Barriers for Translational and Clinical Research”
Laura Odwazny, JD
Senior Attorney, Office for Human Research Protections
Office of the General Counsel, Public Health Division
U.S. Department of Health and Human Services
Rockville, MD
LOdwazny@psc.gov
Speaker - Session(s): B3: Advanced:“Non-Compliance versus Scientific Misconduct” and;
C1: Basic: “Informed Consent in Research”
Jaime Parent, MA, MHS
Vice President, Information Technology
Rush University Medical Center
Chicago, IL
jaime_b_parent@rush.edu
Moderator - Breakout Session C2: Social-Behavioral: “Data Security and Mobile Devices: What Should Institutional Policy Say about Laptops and Other Devices That Move Between Your Office and Home”
Debra M. Parrish, JD
Parrish Law Offices
Pittsburgh, PA
debbie@dparrishlaw.com
Speaker - Session B3: Advanced: “Non-Compliance versus Scientific Misconduct”
Anthony Perry, MD
Associate Professor of Internal Medicine
Director, Johnston R. Bowman Health Center
Rush University Medical Center
Chicago, IL
anthony_j_perry@rush.edu
Speaker - Session A1: Basic: “Historical Overview”
Lainie Friedman Ross, MD, PhD
Carolyn and Matthew Bucksbaum Professor of Clinical Ethics
Professor, Departments of Pediatrics, Medicine, and Surgery
Associate Director, MacLean Center for Clinical Medical Ethics
Department Pediatrics, University of Chicago
Chicago, IL
Lross@uchicago.edu
Speaker - Session C3: Advanced Topic: Special Populations (“Children in Medical Research: Access versus Protection”)
Raj Shah, MD
Assistant Professor, Rush Alzheimer’s Disease Center Assistant Professor
Rush Alzheimer’s Disease Center
Rush University Medical Center
Chicago, IL
raj_c_shah@rush.edu
Moderator - Breakout Session C3: Advance Topic: “Special Populations”
Ryan Spellecy, PhD
Associate Professor of Ethics and Psychiatry
Chairman, Institutional Review Board
Center for the Study of Bioethics
Medical College of Wisconsin
Milwaukee, WI
rspellec@mcw.edu
Speaker - Session C4: Hot/Important: “Emergency Research without Informed Consent”
Julian Solway, MD
Walter L. Palmer
Distinguished Service Professor of Medicine and Pediatrics
Associate Dean for Translational Medicine, Biological Sciences Division
Vice Chair for Research, Department of Medicine
Chair, Committee on Molecular Medicine
University of Chicago
Chicago, IL
jsolway@medicine.bsd.uchicago.edu
Speaker - Session A4: Translational Research: “How it’s done in Chicago: Efforts to Reduce Regulatory Barriers for Translational and Clinical Research”
Paul Song, PhD
Professor, Center for Bioethics
University of Minnesota
Minneapolis, MN
Speaker - Session C3: Advanced Topic: “Special Populations” (“End of Life Research with the Homeless”)
Mark Stein, PhD
Professor of Psychiatry and Pediatrics
Director, Regulatory Support and Advocacy Core, CCTS
The University of Illinois
Chicago, IL
mstein@uic.edu
Speaker - Session A4: Hot: Translational Research: “How it’s Done in Chicago: Efforts to Reduce Regulatory Barriers for Translational and Clinical Research”
Jeremy Sugarman, MD, MPH, MA
Harvey M. Meyerhoff Professor of Bioethics and Medicine
Berman Institute of Bioethics and Department of Medicine
John Hopkins University
Baltimore, MD
jsugarm1@jhmi.edu
Speaker - Plenary Session B: “Managing Financial Conflicts of Interest in Human Subjects Research”
Elyse I. Summers, JD
Director
Division of Education and Development
Office for Human Research Protections
U.S. Department of Health and Human Services
Rockville, MD
elyse.summers@hhs.gov
Speaker - Session(s): “What's New and Important from the Feds?”
B1: Basic: “Human Subjects Protections”
Clyde Wheeler, PhD
Associate Director for Research Compliance
Office of the Vice Chancellor for Research
University of Illinois at Chicago
Chicago, IL
cwheeler@uic.edu
Moderator - Breakout Session B3: Advanced: “Non-Compliance Versus Scientific Misconduct”
Mary Jane Welch, DNP, APRN, MS, BC
Director, Human Subjects’ Protection
Rush University Medical Center
Chicago, IL
mary_jane_welch@rush.edu
Moderator - Breakout Session B1: Basic: “Human Subjects Protections”
JoEllen Wilbur, PhD, RN, CS, FAAN
Professor and Endowed Independence Foundation
Associate Dean Nursing Research & Scholarship
College of Nursing, Rush University Medical Center
Chicago, IL
JoEllen_Wilbur@rush.edu
Speaker - Session B2: Socio-Behavioral: “Engaging the Hard to Engage”
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