MRCT Center Leaning In webinar: Workforce Development

Webinar

Presented on: October 28, 2020, 11:00 AM.-12 noon. ET.

Presented at: MRCT Center Leaning In Webinar Series

Discussion Topic: An MRCT Leaning In webinar focused on Workforce Development. Moderated by Luther Clark, MD Deputy Chief Patient Officer at Merck, we will be joined by MRCT Center’s Sarah White, MPH to review recommendations made in the Achieving Diversity, Inclusion and Equity in Clinical Research Guidance Document. Guest speakers include Racquel W. Bruton, Senior Clinical Operations Lead at Biogen, and Karen M. Winkfield, MD, PhD, Executive Director at Meharry-Vanderbilt Alliance.

Webinar

Slides

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 

April 14, 2021: How to Begin 

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 

MRCT Center Leaning In webinar: Community Awareness, Access, Knowledge

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

PDF

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 

April 14, 2021: How to Begin 

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 

Defining Diversity

Diversity, Inclusion, and Equity in Clinical Research.

Framework:

Developed on: August 2020

Developed by: MRCT Center Diversity Workgroup

We define the term “diversity” to be broad and inclusive. At minimum, it includes:
  • Demographic factors such as sex, race, ethnicity, age, location, genetics etc.
  • Non-demographic factors such as comorbidities, organ dysfunction, concurrent medications, environmental factors, compliance. Among non-demographic factors are those that are historically, socially, and culturally determined.
  • Social factors, and those within the term “social determinants of health,” including education level, economic status, family size, food insecurity, etc.

Examples of Dimensions and Intersections of Diversity

Diversity, Inclusion, and Equity In Clinical Research: Diversity Principles And Suppositions

Framework

Developed on: August 2020

Developed by: MRCT Center Diversity Workgroup

The MRCT Center Diversity Workgroup has developed a set of fundamental principles that help to frame considerations of diverse representation in clinical research. While we recognize that a case-based analysis will be required for each clinical research question, we also believe that these principles will help guide those analyses.