Webinar
Presented on: October 14, 2020, 11:00 AM.-12 noon. ET.
Presented at: MRCT Center Leaning In Webinar Series
Discussion Topic: Participants in clinical research should reflect the population affected by the disease, or those intended to utilize the intervention. Early and active engagement from participants, patients, caregivers, and communities can influence and improve the design and execution of clinical research, including efforts to enhance diversity and inclusion. Further, appropriate and meaningful engagement offers opportunities for outreach to individuals and communities including those underrepresented or underserved in research, addresses priorities that are important for patients and potential participants, and to draws upon the perspectives of the very individuals for whom the research is intended.
Webinar
Related Resources
See related Webinars, maintained on our project specific Diversity, Inclusion, and Equity in Clinical Research website:
October 14, 2020: Community Awareness, Access, Knowledge
October 28, 2020: Workforce Development
November 18, 2020: Study Design, Eligibility, Site Selection, & Feasibility
December 9, 2020: Study Conduct (Recruitment, Retention)
January 13, 2021: Data Standards and Analysis
January 27, 2021: Stakeholder Roles and Responsibilities
May 12, 2021: Inducement or Fair Compensation? Impact on Diverse Participation
June 9, 2021: Improving Inclusion of Persons with Disabilities in Clinical Research
July 14, 2021: Simplifying the Complexity of Translation in Clinical Research