This workshop will help you achieve a paperless system at your site without investing in an expensive clinical trial management system, saving time, money, and space. Speakers will provide interactive demonstrations of paperless subject chart creation and address adverse event adjudication, investigator oversight, electronic binder organization, remote monitoring facilitation, and more. Work in small groups led by subject experts to discuss issues site might face in making the move to paperless and their potential solutions. Leave with the ability to capitalize on the opportunities created through the evolution of electronic systems. Participants are encouraged to bring laptops with Adobe Acrobat Pro if possible for this engaging, hands-on workshop.
To register, select Workshop 004. NOTE: Workshops at not included with Full-Conference Registration and require a separate registration fee.
Contact Hours/CEUs: 3.5 (ACRP)
- Kyusun Cha, CCRC, Research Manager, University of California San Francisco
- Kydanis Clase, Clinical Research Coordinator, Columbia University
- Amanda Alonso, CCRC, Senior Clinical Research manager, Columbia University
- Wanda Truong, MS, Clinical Trials Administrator, Weill Cornell Medicine Comprehensive Weight Control Center