CRAs and Interim Monitoring Visits

Discusses the process and content of a CRA’s interim monitoring visit.

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About this Webinar

The Clinical Research Associate’s (CRA) duties are to ensure that the clinical trial is conducted according to the protocol, good clinical practice, and other applicable guidelines. Interim monitoring visits are one of the essential tasks that CRAs carry out. This webinar details the functions of the CRA during an interim monitoring visit and highlights common findings. Special attention is given to the interactions between the CRA and study team members. Finally, the webinar explains some of the core traits of an effective CRA.

Webinar Demo:

Release Date: July 13, 2023

Language Availability: English

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

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

CRAs and Interim Monitoring Visits

Presented by: Divyesh Kukadiya, MS, CCRP - Children’s National Hospital

Learning Objectives:

  • Describe the primary functions of a CRA.
  • Detail the role that CRAs play in conducting interim monitoring visits.
  • Discuss the range of possible findings from an interim monitoring visit.
  • Explain the core traits of an effective CRA.

Recommended Use: Required
ID (Language): 20965 (English)

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