The Association of Clinical Research Professionals

Webinar—Monitoring Investigator-Initiated Trials

Event Date: June 9, 2021, 12:00-1:00 PM ET

Registration Deadline: June 8, 2021 11:59 PM ET


  • Abby Statler, Director of Research Quality and Safety, Dartmouth-Hitchcock Medical Center

Pricing With Contact Hours

Member: $15 | Nonmember: $75

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This course is approved for 1.0 ACRP contact hours. Accreditation Details

Pricing Without Contact Hours

Member: $0 | Nonmember: N/A

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Learn how to effectively design and implement a monitoring program for investigator-initiated trials (IITs). Attendees will gain valuable knowledge regarding how to create a process for internally assessing the quality of IITs. Templates, workflows and more will be shared, giving the audience essential tools to adapt the proposed program to their own institutional needs.

Upon completion of this Webinar, attendees should be able to:

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

Additional Investigator-Initiated Trial Training from ACRP

Looking for more training on Investigator-initiated trials? Explore these on-demand Webinar Replays and recorded sessions: