Interactive lecture and hands-on workshop training methods will provide you with the tools to design and manage clinical studies.



Overview

• Good Clinical Practices (GCP)

• Clinical research methodology and its role in drug development

• CRA’s role in clinical research

• Monitoring clinical trials to ensure valid and useful study data

• Basic protocol development



Learning Objectives:

At the conclusion of this course, participants should be able to:

• Describe the basic clinical research elements in drug development

• Recognize the basic elements of clinical trial methodology in the conduct of clinical studies

• Identify and select qualified clinical investigators

• Recognize the requirements for safety surveillance

• Recognize the elements of protocol development



Target Audience:

• Clinical research associates and clinical study monitors with less than two years of experience

• Administrative support personnel

• Study support personnel



Event Code:
11920