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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This Webinar will outline the processes and procedures needed to design and implement a monitoring program for investigator-initiated research studies, with a specific focus on sponsor-investigator studies that involve an Investigational New Drug or Investigational Device Exemption.

Designing a program to enhance the quality of investigator-initiated research is essential to achieving excellence, particularly within the Academic Medical Center setting. Understanding the fundamental objectives, processes, and procedures required to effectively monitor such studies are crucial to the success of any research program.

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

  1. Gain specific knowledge around how to design and implement a monitoring program
  2. Review components and dissemination of findings from a strategic study selection (for monitory)