Virtual Clinical Trials: Monitoring and Auditing During the Pandemic - A Real World Case Study

Presented December 16, 2020

Presenters shared a case study of virtual monitoring and auditing, which has been in effect at Memorial Sloan Kettering Cancer Center (MSK) since 2011 and has become especially relevant during the COVID-19 pandemic.
 
The webinar was presented by Karima Yataghene, MD, director of clinical research quality assurance, and Michael Buckley, MS, MBA, enterprise clinical research innovation manager, both of MSK.

Buckley and Yataghene Slides 

Presented by Karima Yataghene, MD, and Michael Buckley, MS, MBA
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Implementing the Shared Investigator Platform

Presented June 18, 2020

Members of AACI's Shared Investigator Platform (SIP) Task Force shared experiences and suggested workflows for the successful implementation of the SIP. The webinar was moderated by Hobs Apell, senior executive director, Clinical Trials Office at The University of Kansas Cancer Center. Presenters included Lindsay Casetta, CCRP, quality assurance and education manager, Barbara Ann Karmanos Cancer Institute; Jessica Moehle, CCRP, director of operations, Clinical Trials Office, Huntsman Cancer Institute; and Kendra Todd, MBA, operations manager, OHSU Knight Cancer Institute. Lestter Cruz Serrano, MD, medical affairs director, Cognizant Life Sciences—the company that developed the SIP—offered guidance for implementing the SIP platform.

Perspectives on Implementing an eRegulatory System

Presented December 10, 2019

A webinar in which two clinical trials administrators described their cancer centers' electronic file management solutions. The webinar was presented by Brieana Marino, MA, regulatory manager at UPMC Hillman Cancer Center, and Cary Passaglia, MSRC, CCRP, administrative director of clinical operations at Robert H. Lurie Comprehensive Cancer Center of Northwestern University.

Perspectives on Implementing an eRegulatory System 

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