The Role of Data Managers in Clinical Trials

The webinar details the functions of clinical data managers in the production of clinical trial results.

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About this Webinar

The webinar highlights the importance of clinical data managers during the conduct of a clinical trial and outlines the process of collecting, managing, analyzing, and reporting clinical trial data from study startup through study closeout. The webinar also discusses the relationship between clinical data managers and principal investigators, clinical research coordinators, and clinical research associates.

Release Date: August 22, 2024

Language Availability: English

Suggested Audiences: Clinical Data Managers, Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Investigators, Research Administrators, Sponsors, Students

Organizational Subscription Price: Included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person


Webinar Content

The Role of Data Managers in Clinical Trials

Iris Rigor, MPH, CCRP - National Cancer Institute, NIH

Learning Objectives:

  • Explain the importance of data management in clinical trials.
  • Describe the roles and responsibilities of clinical data managers (CDMs) in clinical trials.
  • Discuss the ways in which data managers interact with other clinical trial stakeholders such as clinical research coordinators (CRCs) and clinical research associates (CRAs).

Recommended Use: Required
ID (Language): 21250 (English)


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