The Association of Clinical Research Professionals

Webinar Replay: How to Ensure Study Compliance and Integrity through Training and Delegation of Authority

Contact Hours: 1 (ACRP or CBRN)

Member: $25 | Non-Member: $75

Webinar Replay Expiration: July 25, 2018

Webinar Replay Expiration Date: July 25, 2018

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According to the FDA and OHRP, the Principal Investigator (PI) is responsible for all study conduct. However, in the day of complex study designs it is impossible for the PI to directly conduct all aspects of a research study. Therefore, qualified and reliable staff must be employed to ensure the study is carried out according to the protocol. Attendees of this webinar will understand the regulatory requirements of investigator oversight, as well as gain tips for ensuring investigators are properly engaged with delegated duties; study staff entrusted with study conduct are properly trained; and delegation of authority documentation is maintained.

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

  1. Describe the investigator’s responsibility for study conduct and explain the delegation of authority process
  2. Explain how to obtain and maintain ethically responsible delegation of authority
  3. Implement a system to document delegation of authority in a regulatory-compliant manner

Speaker Wendy Tate, PhD, MS, is the Director of Data Analytics for Nimblify, a Forte Research Systems company. Wendy’s work is focused on the analytical evaluation of clinical research administration, including the development and testing of quantitative methods to measure and assess protocol feasibility and workload.

Speaker Mariette Marsh, MPA, CIP, is the Director of the Human Subjects Protection & Privacy Program for the University of Arizona. Mariette has been involved in human research oversight for 18 years at multiple institutions. She received her MPA in Public Affairs, specializing in public policy, from the University of Missouri-Columbia in 2005.

Bring this Program to Your Team!

Bring the quality and effectiveness of this program to your entire clinical research team! We’re ready to help you achieve your organization’s goals and promote excellence in clinical research. Get in touch today and we’ll get started!

Jenna Rouse

Director, Business Development
Talent Onboarding & Staff Development
+1.703.254.8109

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