image goes here
Racial Diversity in Clinical Trials: Building Trust in Participant Engagement
While racial and ethnic diversity in clinical trial participation has long been an issue, COVID-19 vaccine trials have brought this issue to national attention. How can the research community address the root causes for lack of diversity? What actions can be taken to build trust among socioeconomically, racially, and ethnically diverse populations and initiate change? What role do community healthcare centers play in establishing that trust?
Join us for a panel discussion of ways we can unlock the inherent trust between patients and community healthcare providers to encourage diverse representation in clinical trials. Experts from research organizations and community health centers discusses ways biopharma and health centers can come together to improve equity in research.
Learning Objectives:
- Identify ways to overcome root causes of research inequity and increasing diverse enrollment in clinical trials
- Discuss the role of community health centers and how they may be the “missing link” in helping ensure new therapies are safe and effective for the entire US population
- Analyze data that impact negative perceptions regarding research participation and how it could influence decision making for initiatives that drive change
- Describe actions that can be taken across the research ecosystem, including protocol design, trial modalities and use of technology, community engagement, and more
Presented By
Michele Russell-Einhorn
JD
Chief Compliance Officer and Institutional Official
Advarra
Jonathan Jackson
PhD
Director of the Community Access, Recruitment, & Engagement
Research Center, Massachusetts General Hospital; Harvard Medical School
Rajan Sonik
PhD, JD, MPH
Director of Research
AltaMed Health Services
Melissa Opraseuth
PharmD
Chief Operating Officer
par8o
DATE: July 8, 2020
Time: 1 pm ET | 10 am PT
Duration: 1 hour