Hosted by the Human Research Projection Office, Office of the Vice Chancellor for Research, Center for Clinical Studies and Bernard Becker Medical Library
A Zoom link will be provided to all registrants prior to the workshop.
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 individuals 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 and mHealth Research Core (mHRC)
- Andrea Morris
Manager, Human Research Quality Assurance Program, OVCR
- Mitchell Saulisbury-Robertson
Assistant Director, Social Behavioral Research & Expedited Review, HRPO
- Chris Sorensen
Senior Support Scientist, Bernard Becker Medical Library
- Jeanne Velders
Executive Director, HRPO