The Association of Clinical Research Professionals

Clinical Trial Monitoring Basics

This training program answers the fundamental question: What IS clinical trial monitoring?

After answering that question, this course builds on that content to examine various monitoring types and approaches, including site initiation visits, routine monitoring visits, and risk-based monitoring.

Clinical Trial Monitoring Basics is a course beneficial to all clinical research professionals involved in the conduct of subject visits and data review, collection, and recording, as well as those involved in clinical trial monitoring activities.

Upon completion of this training program, participants should be able to:

  • Define monitoring, and who is responsible for monitoring.
  • Understand the purpose of monitoring.
  • List the responsibilities of the monitor.

This course helps clinical researchers of all types builds competency in Communication and Teamwork, Data Management and Informatics, and Study and Site Management. Explore Competencies >

Approved for 1.5 ACRP Contact Hours | Available 1 Year from Enrollment Date