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
