Archive: Managing CRAs to Improve Performance and Study Outcomes

June 21, 2018 | Barnett International Recording

Web Seminar Archives are available in either USB Flash Drive or DVD Format.

Archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.

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$625.00

Course Description

Monitoring a clinical trial is a required activity completed by sponsors of FDA regulated research that significantly affects the outcomes of product development and approval. Effectively managing the performance of Clinical Research Associates (CRAs) by sponsors is essential. Performance Management and Improvement is a science involving logical processes and applications. This web seminar will present the concepts of the Human Performance Improvement (HPI) Model and apply it directly to the management of the CRA to promote improvements. The HPI CRA Management Model will be presented and applied via case scenarios for better understanding.

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Learning Objectives

  • Define the Human Performance Improvement Model
  • Recognize an HPI CRA Management Model
  • Apply the model into current practice: Proactive CRA management
  • Apply the model into current practice: Managing CRA performance issues
  • Analyze case scenarios

Who Should Attend

  • Project Managers
  • Lead Clinical Research Associates
  • Clinical Research Associate Managers

Instructor

Tabitha Westbrook, M.A., LPCA, CCTP RQAP-GCP

Click here for complete trainer biographies

 

Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.