“Project Management in the Field”
Master Class Series
October 4 - 6, 2022
2:00 PM - 4:45 PM
Location
Remote via Zoom
Calendar
Download iCal FileProgram Description
This interactive workshop, comprised of 2 half-day sessions, is designed to increase research coordinators’ knowledge and confidence regarding project management, with a focus on study implementation.
The full program agenda can be found below.
Moderator
Rachel Olech, Senior Regulatory Specialist, CCTS Regulatory and Bioethics Core
Master Class Series
The CCTS Master Class series helps clinicians, research coordinators/specialists and other health research personnel develop a better understanding of conducting human subjects research at UIC.
Completion of the Master Class series is a requirement of the RC+ Certificate Program, a comprehensive educational certificate program for UIC research personnel involved in clinical, translational, community-based, social and/or behavioral sciences. Learn more about the RC+ Certificate Program.
Date posted
Sep 13, 2022
Date updated
Sep 19, 2022
Program Agenda Heading link
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Day 1 Agenda
2:00-2:10pm
Welcome / Introduction to course
2:10-2:40pm
Data Security
Himanshu Sharma, Director, Advanced Cyberinfrastructure for Education and Research (ACER)
UIC Technology Solutions2:40-3:20pm
Study documentation
Lauren Castro, RN, MSN, Director of Clinical Research Operations
UIC Breathe Chicago Center3:20-3:30pm
Break
3:30-4:00pm
Conflicts of Interest and Commitment
Jacquelyn Jancius, Director Conflict of Commitment and Interest
Office of Vice Chancellor for Research4:00 – 4:30pm
Panel Discussion – Participant Management: Stories from the Front
This discussion will feature experienced research personnel at UIC, who will share their stories related to managing research participants and navigating research activities.4:30 – 4:45pm
Wrap Up
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day 2
Day 2 Agenda
2:00-2:10pm
Introduction
2:10 – 2:35pm
Fundamentals of Survey Administration (pre-recorded)
Kelly O’Shea, MPH, Associate Director of Evaluation and Tracking
UIC Center for Clinical and Translational Sciences2:35-3:00pm
An Overview of Research Misconduct: Fabrication and Falsification
Rick Gemeinhart, PhD, Professor of Pharmaceutics and Bioengineering
UIC Research Integrity Officer & Associate Vice Chancellor for Research3:00 – 3:25pm
Coordinating Sponsor and Regulatory Audits
Annette Kinsella, RN, CRC, QA Education Specialist
University of Illinois Cancer Center, Clinical Trials Office3:25-3:50pm
Panel Discussion – When something goes wrong
This discussion will feature research and regulatory experts, and will provide an overview of the identification, prevention, management, corrective and preventive action plans (CAPA), reporting, and notes to file related to problems associated with the conduct of research.3:50 – 4:00pm
Wrap-Up