Hosted by the Human Research Protection Office, Office of the Vice Chancellor for Research, Center for Clinical Studies and Bernard Becker Medical Library
This workshop will give researchers and research staff an opportunity to share experiences, challenges and best practices around the use of e-consent.
By sharing with others, we hope attendees will continue to develop and improve their e-consent processes. In addition to conversations about e-consent platforms, we encourage discussions about the actual process of obtaining consent and feedback obtained from research participants. The workshop will consist of opening remarks by the groups listed below followed by small break out session and large group discussion. Please be prepared to share your experiences with the group for a lively and informative discussion!
Katie Keenoy, Clinical Research Specialist, Center for Clinical Studies
Andrea Morris, Manager, Human Research Quality Assurance Program, OVCR
Mitchel Saulisbury-Robertson, Assistant Director, Social Behavioral Research and Expedited Review, HRPO
Chris Sorensen, Senior Support Scientist, Bernard Becker Medical Library
Jeanne Velders, Executive Director, HRPO