Best Practice Hour Seminar Archives
Seminar Archives by Year
2024
January 16, 2024
Preparing for an Audit/Inspection
Annette Kinsella, RN, CCRC, QA Education Specialist, University of Illinois Cancer Center
Danielle Cavanaugh, MLS, Clinical Research Compliance Specialist, UIC Office of the Vice Chancellor for Research
Erin Vidra, MS, CHRC, Director, Research Compliance, UIC Office of the Vice Chancellor for Research
2023
December 19, 2023
Data Management for Clinical Trials
Andrew Boyd, MD, Associate Professor, Biomedical & Health Information Sciences, Associate Director, Informatics Integration, Education & Collaboration, Consultant, CCTS Biomedical Informatics Core
October 17, 2023
Adverse Events/Serious Adverse Events & Unanticipated Problems Identification & Documentation
Annette Kinsella, RN, CCRC, QA Education Specialist, University of Illinois Cancer Center,
September 19, 2023
Single IRB
Jovana Lombardo, MPA, IRB Associate Director/Single IRB Point of Contact, UIC OPRS
August 15, 2023
Team Science & Communication
Amy Kennedy-Krage, MBA, MSW, Co-Director of Clinical Research Operations, CCTS Clinical Research Center
July 18, 2023
Top 10 Reasons for Modifications from the IRB
Rachel Olech, Senior Regulatory Specialist, CCTS Regulatory and Bioethics Core
June 20, 2023
EPIC Updates
Andrew Boyd, MD, Associate Professor, Biomedical & Health Information Sciences, Associate Director, Informatics Integration, Education & Collaboration, Consultant, CCTS Biomedical Informatics Core
May 16, 2023
Informed Consent of Special Populations
Darlene Kitterman, Director, Clinical Trials Office, University of Illinois Cancer Center
Arielle Breanna Guzman, Senior Clinical Research Coordinator, Clinical Trials Office, UI Cancer Center
April 18, 2023
Five W’s of the Investigational Drug Service (IDS)
David Chan, PharmD, PhD, Manager, Investigational Drug Services, Clinical Assistant Professor, UIC College of Pharmacy
March 21, 2023
REDCap Introduction for Data Collection
Rachel Lane, MS, Research Specialist, CCTS Biostatistics Core
February 21, 2023
Recruitment and Retention from CEAB Members’ Perspective
CCTS Community Engagement Advisory Board panel
January 17, 2023
IND/IDE’s & Regulatory Pathways
Darlene Kitterman, MBA, Director, University of Illinois Cancer Center, Clinical Trials Office
2022
November 15, 2022
Demystifying the Contract Review Process for Industry Sponsored Clinical Trials
Brenda Barrie, CRA, Clinical Research Contracts Specialist, UIC Office of Sponsored Programs
October 18, 2022
Clinical Trial Designs
Ryan Rodriguez, Clinical Associate Professor, UIC College of Pharmacy
September 20, 2022
Research Billing Review & Set-Up Process
Scott Kennedy, Assistant Director, UIC Clinical Research Finance Office (CRFO)
July 19, 2022
Clinical Trial Budgets
Mike Isaac, Assistant Director for Research Operations, University of Illinois Cancer Center Clinical Trials Office
June 21, 2022
ClinicalTrials.gov
Annette Kinsella, RN, CCRC, QA Education Specialist, University of Illinois Cancer Center Clinical Trials Office
May 17, 2022
Introduction to UIC Research
Charles Hoehne, Assistant Director, Education, UIC Office for the Protection of Research Subjects
Barbara Corpus, Associate Director, External Relations, UIC Office for the Protection of Research Subjects
April 19, 2022
UIC Clinical Trials Review Committees: What, When, & How?
Darlene Kitterman, MBA, Director, University of Illinois Cancer Center Clinical Trials Office
March 15, 2022
Study Startup
Erin Vidra, Regulatory Manager, University of Illinois Cancer Center Clinical Trials Office
January 18, 2022
Study Financial Management
Michael Isaac, Assistant Director of Research, Clinical Trials Office