Christopher M. Ryan, Ph.D. IRB Director

Slides:



Advertisements
Similar presentations
Is it Research?. Is It Research? 2 Elements –The project involves a systematic investigation –The design (meaning goal, purpose, or intent) of the investigation.
Advertisements

Human Subjects Training Requirements All researchers, advisors, and research assistants must complete training. You must have an overall passing rate of.
Annual IRB Member Training October 2010 Research Participant Compensation John Stillman Director Institutional Review Board University of Utah.
FERPA and IRB: Implications for Testing Centers Judith W. Grant, Ph.D.,CIP NCTA Conference San Antonio, Texas August 6, 2009.
Recently Issued OHRP Documents: Guidance on Subject Withdrawal and Draft Revised FWA Secretary’s Advisory Committee on Human Research Protections October.
DO NO HARM IRRB Presentation Purposes Responsibilities Processes NLU IRRB Home page.
Exempt Research Mary Banks BS, BSN IRB Director CRC IRB and BUMC IRB.
Denise Viator Technical Assistance Project Manager Oak Ridge Associated Universities DOE Human Subject Working Group Workshop December 1, 2011 National.
John Naim, PhD Director Clinical Trials Research Unit
IRB Basics Helen Panageas New York University School of Medicine Institutional Review Board Portion of slides courtesy of Suzanne M. Smith, University.
Human Subjects Protection in Research Carnegie Mellon University Regulatory Compliance Administration 5000 Forbes Avenue, UTDC Bldg., Rooms 108 & 109 Pittsburgh,
UM-FLINT INSTITUTIONAL REVIEW BOARD CERTIFICATION IN HUMAN SUBJECTS PROTECTION.
Office of Research Integrity Office of Research Integrity Orientation Session November 8, 2012 ECSS
CITI: Collaborative Institutional Training Initiative.
Cornell Evaluation Network The Use of Human Participants in Research Office of Research Integrity and Assurance ~ May 14, 2007.
Responsible Conduct of Research (RCR) What is RCR? New Requirements for RCR Who Does it Affect? When? Data Management What is the Institutional Plan? What.
The Institutional Review Board: A Community College Toolkit Dr. Geri J Anderson.
Office of Research Integrity and Compliance March 2011.
Danielle Davidov 12/07/2012.  The purpose of CITI Training is to prepare you to conduct research with human subjects  This training will educate you.
The Linguistics Department Institutional Review Board Committee Silvina Montrul, chair Fred Davidson Irene Koshik Ryan Shosted September 22, 2008.
Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student.
Dustin Yocum, MA Institutional Review Board University of Illinois HUMAN SUBJECTS RESEARCH.
IRB Process Overview Ling Wang IRB Representative Graduate School of Computer and Information Sciences.
Introduces ePIRATE electronic Portal for Institutional Research at ECU East Carolina University Office for Human Research Integrity.
Johns Hopkins Bloomberg School of Public Health Institutional Review Board Brown Bag Series February 7, 2007 CITI – What is It & Why Do I have to Do It?
What Institutional Researchers Should Know about the IRB Susan Thompson Senior Research Analyst Office of Institutional Research Presented at the Texas.
WELCOME to the TULANE UNIVERSITY HUMAN RESEARCH PROTECTION OFFICE WORKSHOP for SOCIAL/BEHAVIORAL RESEARCH (March 2, 2010) Tulane University HRPO Uptown.
NAU New CITI Account Guidance for Signing up Prepared by: Christine Melton-Lopez, IRB Associate.
Paul Hryvniak MS, CIP Alyssa Speier, MS, CIP September 30, 2014 Student Human Research Education Session Tel:
Ask the IRB: Student International Research Edition Christopher Ryan, PhD, CIP Director, Pitt IRB Professor of Psychiatry, Psychology, and Health & Community.
Human Subjects Research Training Having a Successful CITI Experience.
Research Ethics Office of Research Compliance. Responsible Conduct of Research (RCR) Covers 9 content areas –Animal Subjects (IACUC) –Human Subjects (IRB)
Collaborative Institutional Training Initiative (CITI) citiprogram.org Georgia Institute of Technology.
Confidentiality Training
Overview of COI training requirements
Brief Overview of IRB and Human Subject Protections Issues at the University of Richmond Dr. R. Kirk Jonas Chair, University of Richmond Institutional.
COCE Institutional Review Board Academic Spotlight
Principal Investigator Responsibilities
University of Central Florida Office of Research & Commercialization
Rich DeMary / Tammy Patton
The Protection of Human Participants in Research
Confidentiality Training
Research with human participants at Carnegie Mellon University
SOU Institutional Review Board
Dining with Diabetes IRB Training 2017.
Conflict of Interest in Research
For investigators planning to conduct human participant research
Getting Started with Human Subjects Research
Overview of COI training requirements
The CITI Program Mission Statement Training on regulations with CITI
The Importance of Ethics and the Protection of Subjects By Westley R
University of Central Florida Office of Research & Commercialization
AAHRPP Accreditation Welcome to the University of Georgia’s presentation for accreditation of the human research protection program (HRPP). This presentation.
© 2016 The McGraw-Hill Companies, Inc.
HB4034 – Duplicate Batch Process
Anca Miron, PhD IRB Chair, UW Oshkosh Kelly Schill, BS, CIP
SOU Institutional Review Board
Updates to Expedited Review Procedures
2/1/2019 3:33 PM Tennessee State University Institutional Review Board
Office of Sponsored Programs
Human Participants Research
Office of Research Integrity and Protections
Valdosta State University
Event Reporting in Human Subjects Research
The CITI Program Mission Statement Training on regulations with CITI
Getting Started with Human Research
Casey Hyatt, Secretary Institutional Review Board
Research with Human Subjects
Introduction to the USC Human Subjects Protection Program
Research Compliance: Protections for Research Subjects
Presentation transcript:

Christopher M. Ryan, Ph.D. IRB Director ryancm@upmc.edu Human Subjects Research Update New CITI Training Modules Child Clearance Requirements WePay Secrets Christopher M. Ryan, Ph.D. IRB Director ryancm@upmc.edu

Collaborative Initiative Training Institute (CITI): Why the Change? Federal regulations mandate training in human subject protections CITI Program: “Gold standard” for internet-based research ethics training Accepted by virtually all institutions/agencies Single source for all training New courses continually developed and existing courses updated

General Information Pitt/UPMC: Continue to use HSConnect authentication Every user must have a HSConnect account Special portal to access CITI courses www.citi.pitt.edu External Investigators with CITI accounts Obtain credit for previously completed CITI modules that match Pitt requirements (if taken within 2 years) Eliminates redundant training across institutions

New users required to take the CITI courses prior to conducting human subject research or to access OSIRIS Existing users have one year to complete the CITI courses After March 31, 2013, access to OSIRIS will be denied Cumulative passing score of 80% 3-5 hours to complete all modules (some report 7 hours) Re-certification every 3 years CITI ‘Refresher Course’ plus other requirements Reminder notifications sent out automatically

Designated “User Groups” Biomedical Researcher (including all health science students) Social & Behavioral Researcher Undergraduate Student Researcher Optional course for IRB Members

Go to www.citi.pitt.edu

Create a new account or login in with your existing account Do not create a duplicate account. If you are unsure, email us irb@pitt.edu

Creating or merging your CITI account

Linking your existing CITI with Pitt

Access the course modules Example: Student Researchers

Social/Behavioral Human Subjects Curriculum Belmont Report History and Ethical Principles Defining Research with Human Subjects The Regulations & Social/Behavioral Science Assessing Risk in Social/Behavioral Research Informed Consent Privacy & Confidentiality Conflicts of Interest Two Additional Electives

Social/Behavioral Responsible Conduct of Research Curriculum Responsible Mentoring Introduction to the Responsible Conduct of Research Research Misconduct Data Acquisition, management & Sharing Publication Practices and Responsible Authorship Collaborative Research + 1 Elective module

Additional Continuing Education Requirements Required to attend at least 3 continuing education hours (CEUs) in a 3-year period specifically related to human subject protection or ethics Examples may include: IRB programs (i.e., Ask the IRB) IRB board member attendance ACRP programs Keep records of attendance in your file

FAQs I took the VA version of CITI last year. Is that acceptable at Pitt or should I take it again? As an administrator, how do I verify which courses have been completed by my faculty? I conduct both biomedical and behavioral research. Do I have to complete both courses in CITI? Will we receive reminders when our CITI courses are close to expiring? According to the Provost, all faculty must take the Research Integrity Module and the COI module. If I’ve taken the CITI modules, is that sufficient?

Child Clearance Requirements

New Question Added to OSIRIS It is the responsibility of the principal investigator to ensure that all research staff have these clearances prior to any interaction with children. Act 33; Act 34; FBI Criminal Background Check Contact Human Resources at 412-624-8150 for assistance with this process. OGC Contact: Alan Pittler

FAQs I called Human Resources and they said I was “grandfathered.” Does that mean that no clearances are required? I have an ongoing study. Do I have to stop the study until everyone has their clearances? We are starting a new study. Do I have to wait until all staff have these clearances? We provide ‘babysitting’ for our subjects; does that staff member need these clearances?

FAQs, cont. My secretary greets the kids when they come in but otherwise isn’t involved with the research. Clearances Required? I am interviewing children over the telephone. Clearances Required? I am conducting on-line surveys of children. Clearances Required? I am doing a medical record review on children. Clearances Required? Do these clearances ever expire?

WePay Facts You May Not Know I am the ONLY person at the IRB who addresses WePay issues SSNs must be collected unless a ‘waiver’ is requested E-mail me with request Subjects cannot receive more than $100 in a year Exception: certain studies (e.g., spousal abuse) where receipt of 1099 could lead to harm

Gift cards ordinarily cannot be used ‘Man in the Street’ option E-mail me for an exception (granted infrequently) ‘Man in the Street’ option ‘Petty cash’ approach Can be used to purchase gift cards (but…) Investigators are required to maintain records documenting who received what when Names may not be required, but info is needed to ensure that subjects actually participated Amazon gift codes may be possible…

Upcoming Education Programs Building Bridges: Research Around The World National conference on international research co- sponsored by Pitt, CMU, VA Healthcare System, and the federal Office of Human Research Protections Sheraton Station Square Friday, June 22, 2012