On-Demand Webinar

Diversity and Inclusion: Who is Responsible - Site, CRO or Sponsor?

Attaining a diverse trial patient population is crucial to the success of any clinical trial. But who is truly responsible for maintaining a diverse and inclusive participant database?

In this webinar, Judy Galindo, Monica Cuitiva, Ashley Margo, Dan Sfera, and Chris Sauber, the Co-Founders of Latinos in Clinical Research, discuss why it’s important to recruit diverse patients of all backgrounds and why protocols should be more inclusive. Learn from site owners and those involved within a site level, their perspectives, experience, and feedback.

Learning Objectives:

  • Learn about the importance of inclusive protocols
  • Discuss who is responsible for maintaining a diverse participant database
  • Leverage best practices from peers in the clinical research industry 

Presented By

Judy Galindo

Co Founder
Latinos in Clinical Research

Monica Cuitiva

Co-Founder
Latinos in Clinical Research


Ashley Margo

Co-Founder
Latinos in Clinical Research


Chris Sauber

Co-Founder
Latinos in Clinical Research

Dan Sfera

Co-Founder
Latinos in Clinical Research

 

Who should watch?

This content applies to operational staff, including leadership, from academic medical centers, cancer centers, and health systems.

CE Credits

Attendance at this session has been approved for 1.00 contact hour of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.

This session meets the Certified IRB Professional (CIP) recertification guidelines for a maximum of 1 credit.

Provider approved by the California Board of Registered Nursing, Provider Number 17600, for 1 contact hour. This documentation must be retained by the licensee for a period of 4 years after the course concludes.

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.

If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements.

Certificate of Attendance

After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.

DATE: August 3, 2021
Time: 2 pm ET | 11 am PT
Duration: 1 hour

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