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Increasing Trial Diversity: Steps to Improve Trust Among Diverse Populations

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Date and Time: November 5, 2020 @ 12:00 PM ET


Contact Hours: One contact hour will be issued.


Presenters:

Robin Heiskell, Head of Site Partnerships 

Liz Beatty, Chief Strategy Officer 

Karri Venn, President of Research, LMC Manna Research


Description

Diverse patients are currently underrepresented in clinical trials and the FDA is encouraging sponsors to prioritize meeting patient diversity targets in clinical trials. Black Americans who make up 20% of U.S. multiple myeloma patients and are twice as likely to be diagnosed, only accounted for 4.5% of participants in multiple myeloma trials since 2003. The FDA launched guidance to have trial subjects reflect the patient population that will take the medication once approved, but that starts with increasing trust in clinical trials among diverse populations.  
Learning Objectives
Join clinical leaders at Inato and LMC Manna Research for a webinar to learn: 
Results from an Inato survey of over 250 clinical research sites and how diversity can be improved 
Tactical advice for how to include diverse patient populations in upcoming trials 
The latest FDA guidance on having trial subjects reflect the patient population taking the medication

Presenters:

Robin Heiskell, Head of Site Partnerships 

Liz Beatty, Chief Strategy Officer 


​Karri Venn, President, Research LMC Manna Research

Karri Venn brings over 20 years of clinical research experience working at LMC Manna Research.  Ms. Venn has brought experience, knowledge and drive to many of the positions held at LMC Healthcare.  In 2006, Ms. Venn was promoted to Director, Research of LMC Clinical Research and subsequently in 2015 to President, Research of LMC Manna Research with a key responsibility of integration of Manna with LMC clinical sites to create the largest clinical community research site network in Canada.  In total, there are 20 sites that include therapeutic expertise in all phases of research including real world/big data. 

Ms. Venn has led the project management teams for > 1500 clinical trials and led the response to > 50 Sponsor & Regulatory audits.  LMC Manna has become a reputable program and has received the distinct award as a Centre of Excellence in Diabetes clinical research, PRIME status with IQVIA, awarded in the Top 50 Great Places to Work for Canada and SPRIA winners at the 2017 SCRS conference.  A founding member of hyperCORE International a leading Super Network of clinical sites which comprises of 80 sites, 5 countries and 9 site networks.

Ms. Venn has been certified in project management through the Project Management Institute, as well as longstanding certification as a Clinical Research Coordinator and Diabetes Educator.

Today, she is a founding Board member of the Canadian Association of Independent Clinical Research Sites (CAICR) and great supporter of both Society for Clinical Research Sites (SCRS) & Association of Clinical Research Professionals (ACRP).

Society for Clinical Research Sites, Inc. is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center’s Commission on Accreditation.


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To obtain your Contact Hours for this webinar:

  1. The webinar must be watched in its entirety.
  2. The post webinar survey immediately following this webinar must be completed in its entirety.
  3. Your contact hour certificate will be sent to you within 30 days of you viewing this webinar.
  4. The contact hour certificate will be sent to the email address provided when you registered.

Planners, presenters, faculty, authors, and content reviewers do not have any relevant financial relationships with any commercial interest.

This webinar does not imply any endorsement of products or services by the Society for Clinical Research Sites or ANCC.

The materials and recording of this webinar will be available for one year as an archive, but will not award any contact hours.


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