23/07/2022
Don't miss this online event!
Diversity in clinical and public health research is vital to ensuring that medications and initiatives meet the needs of multiple populations.
In this webinar Danielle Campbell will discuss her research and the value of meaningful inclusion.
Register in advance:
https://us02web.zoom.us/meeting/register/tZYvde2prj8qE9NAKNYS08L_Bzn8KKTp9Udn
Danielle M. Campbell has extensive experience in infectious disease-related work, including the clinical and social sciences of HIV cure-related research, prevention and treatment, and recently SARS-CoV-2. The focus of Danielle’s work has been examining the influence of structural systems and paradigms of power on the production of health inequities among racial/ethnic and sex/gender minority populations living with and affected by HIV/ AIDS and other marginalized populations with an emphasis on women and girls. Danielle is a community organizer for HIV/ AIDS and sexual and reproductive
health, rights, and justice awareness policies and campaigns. She dedicates her energy to serving as a member of a community scientific subcommittee for a global HIV/ AIDS research network, Chair of the American Public Health Association HIV/ AIDS Section, and as a volunteer HIV tester/ counselor aboard a mobile testing unit, and as an educator and promoter of positive sexual health awareness.
Presentation objectives:
Discuss the significance of meaningful inclusion in research as a public health equity issue
Describe the implications of lack representation in research
Overview best practices to advocate for all people to participate in research
Don't miss this webinar on July 25, 2022 11:00-12:00 PM PST hosted by Bridge Clinical Research.
Register in advance:
https://us02web.zoom.us/meeting/register/tZYvde2prj8qE9NAKNYS08L_Bzn8KKTp9Udn
After registering, you will receive a confirmation email containing information about joining the meeting.
In this session, we will: Discuss the significance of meaningful inclusion in research as a public health equity issue Describe the implications of lack representation in research Overview best practices to advocate for all people to participate in research