The Association of Clinical Research Professionals

Monitoring Investigator-Initiated Trials

Learn how to effectively design and implement a monitoring program for investigator-initiated trials (IITs).

This recorded webinar provides participants with valuable knowledge regarding how to create a process for internally assessing the quality of IITs. Templates, workflows, and more are shared, giving participants essential tools to adapt the proposed program to their own institutional needs.

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

  • Identify the key responsibilities of a monitor
  • Describe the components of a monitoring visit (prior to, during, and after the closure of a clinical trial)
  • Determine the process for designing and implementing a monitoring program

Abby Statler, PhD, MPH, MA, Director of Research Quality and Safety, Hitchcock-Dartmouth

Approved for 1.0 ACRP Contact Hours | Expires June 9, 2024