Improving the Clinical Trial Participant’s Experience: From Recruitment through Study Closure

Discusses ways that sponsors, sites, and clinical research organizations can transform the clinical trial experience.

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About this Webinar

The webinar examines strategies that sites, sponsors, and clinical research organizations (CROs) can use to improve participants’ experience in clinical trials. The webinar discusses this experience from the time before the participant volunteers, through the clinical trial journey, to beyond study closure. Listening to participants’ voices and implementing a participant-centric approach to study design, protocols, site operations, and communications can improve the way participants view their involvement and lead to higher retention rates. The webinar explores these areas to gain new perspectives that can be integrated into the clinical trial process.

Webinar Demo:

Release Date: February 24, 2022

Language Availability: English

Suggested Audiences: Clinical Research Coordinators, Clinical Site Staff, Contract Research Organizations (CROs), Principal Investigators (PIs), Research Administrators, Sponsors

Organizational Subscription Price: $300 per year/per site or included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person


Webinar Content

Improving the Clinical Trial Participant’s Experience: From Recruitment through Study Closure

Presented by: Deena Bernstein, MHS - Datacubed Health; Claudia Gomes, MS, ACRP-CP - JEM Headlands LLC

Learning Objectives:

  • Identify strategies sponsors and CROs can integrate into study design to enhance the overall clinical trial participant experience.
  • Discuss best practices for engagement that sites can implement to improve participant experience.
  • Describe tools that can be used to improve retention of clinical trial participants.
  • Explain the importance of listening to the voice of the clinical trial participants to improve their satisfaction with all patient-facing aspects of the clinical trial process.

Recommended Use: Required
ID (Language): 20433 (English)