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Description
Lesbian, gay, bisexual, transgender, queer, intersex, and asexual (LGBTQIA+) people make up approximately 4.5% of the United States population but face worse health outcomes when compared to their non-sexual and gender-minority peers. Despite this, the LGBTQIA+ population remains underrepresented and under-recognized in biomedical and social and behavioral research.
In this webinar, the presenters will discuss LGBTQIA+ health disparities, explore inclusive research data collection methods, and introduce meaningful strategies for IRBs when reviewing studies including LGBTQIA-specific research. Time will be provided for a brief Q&A with the speakers at the end of the session.
Agenda
- LGBTQIA+ health disparities
- Inclusive research data collection methods
- Strategies for reviewing biomedical, social and behavioral, and LGBTQIA-specific research studies
By the end of this session, you should be able to:
- Identify LGBTQIA+ health disparities
- Describe inclusive research data collection methods
- Describe strategies for reviewing biomedical, social and behavioral, and LGBTQIA-specific research studies
This program is geared toward HRPP/IRB personnel and those working in research programs more broadly including HRPP/IRB directors, members, chairs; researchers and research staff; and more.
Continuing Education
Webinar participants holding the Certified IRB Professional (CIP®) credential may apply 1.25 continuing education credits towards CIP recertification. Learn More
90-Day Access Interval
Access to live content will be available for 90 days after the recording is made available. After 90 days, access to the content will be removed, but users will retain access to any certificates of attendance earned. To earn a certificate, one must complete all required sections and complete the certificate section within the 90-day access period. After access has expired, users can purchase an additional 90 days of access.
If you prefer, you can find a paper registration form here. Please send the completed form to registration@primr.org.
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Advarra advances the way clinical research is conducted: bringing life sciences companies, CROs, research sites, investigators, and academia together at the intersection of safety, technology, and collaboration. With trusted review solutions, innovative technologies, experienced consultants, and deep-seated connections across the industry, Advarra provides integrated solutions that safeguard trial participants, empower clinical sites, ensure compliance, and optimize research performance. Advarra is advancing clinical trials to make them safer, smarter, and faster.