E-Consent Workshop: Share your Experiences

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.

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!

Facilitators:

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


May 25th, 2021 12:00 AM - 1:00 PM
Zoom link will be provided before the workshop
United States
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