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Ways to Optimize EMR Recruitment for Oncology Clinical Trial Participants

$79.00 (Non-Member Price)

$0.00 (SCRS members – Included as member benefit, no additional cost)

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Date and Time: June 16, 2020 @ 12:00 PM ET

Contact Hours: One contact hour will be issued.


Marie E. Lamont, Intelliquet


Three absolute truths about the clinical research process exist:  

  1. If we don’t have the right data, we can’t find the right patients.  
  2. When we don’t find patients, we miss recruitment goals, and trials can fail. 
  3. When trials fail, we significantly waste costs and resources and, more importantly, we deny patients much-needed treatment options. 

Many oncology studies with complex criteria continue to fall short of enrollment goals. One promising solution is using Electronic Medical Record (EMR) tools for recruitment. Interrogating the EMR can be an effective and efficient method for clinical trial recruitment, but many challenges still exist. This webinar will explore ways to optimize interrogating the EMR as a recruitment method, including how and when to interrogate EMRs to find patients as well as the tools available for EMR interrogation and how best to evaluate them.

Learning Objectives

  • Key challenges with EMR Recruitment and ways to address them
  • Tools, collaborators and methodologies for optimizing EMR recruitment methods
  • How to evaluate potential solutions and vendors to help ensure success


Marie E. Lamont has more than 25 years as a global biotech leader focusing on many areas, including patient services, strategic planning, business leadership, and commercial operations. She previously headed up a consulting and advisory firm for life sciences and technology. As Interim President and COO at Inteliquet, Marie is responsible for the overall vision and operations with the goal of providing patients and physicians access to the latest and best treatment options and care available. She helps commercialize Inteliquet’s offerings of intelligent technology, insights, and services to improve clinical trial processes, research and translational medicine.

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.


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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