Using A Central IRB At Thomas Jefferson University / Hospital Roseann Talarico Associate Director Office of Human Research.

Slides:



Advertisements
Similar presentations
Central IRBs An IRB Infoshort June Working Definition  A central IRB is one that serves as IRB of record for all of the sites engaged in a research.
Advertisements

My Sponsor Wants to Know if I Can Use a Central IRB An Introduction to Using a Central/Commercial IRB at MSSM.
Changes in Reporting Mandatory COI training Lower threshold for disclosure Required annual disclosure (and amended disclosure if changes occur) Mandatory.
Proposal Submission 101. Proposal Timeline As soon as you have decided to submit, notify our SPPD contracts and grants coordinators, Nicole Burelli and.
UTHSC IRB Donna Hollaway, RN, CCRC 11/30/2011 Authority to Audit 45 CFR (e) An IRB shall conduct continuing review of research covered by this.
Proposals Job Aids EE Cluster Training Jerry Kirk.
Multisite Human Subjects Research CUNY HRPP Coordinator Training October 19, 2012.
Submission to Approval What happens to my protocol once I submit it to the HIC office.
Exempt Research Mary Banks BS, BSN IRB Director CRC IRB and BUMC IRB.
November 10, Office of Research Administration: Clinical Research Contracting Presented to: Research Administration Professionals Group Patricia.
Instructions for VCU’s Internal Approval Form Form is required to obtain Authorized Official’s signature on proposals and awards OSP – 8/2006.
Central IRBs: Ceding IRB Oversight
End User Changes GO LIVE May 13, 2010 PS Grants Implementation.
Conflict of Interest Policy Implementation October 23, 2014.
University of Miami Office of Research Compliance Assessment Lynn E. Smith, JD, CIM, CIP Johanna Stamates, RN, BA, CCRC With assistance from Elizabeth.
UC DAVIS OFFICE OF RESEARCH Overview of Good Clinical Practices (GCP) Investigator and Study Team Responsibilities Miles McFann IRB Administration Training.
Welcome To INSPIR Training Please be sure Please be sure to sign- in to sign- in Please be sure you try to log – on to INSPIR before you leave Please be.
VHA Handbook What’s new. General Requirements for Informed Consent A Legally Authorized Representative may not always qualify as a ‘personal representative’
Western Oregon University INSTITUTIONAL REVIEW BOARD.
Study Closure Process Entropy is not a method Rachel Sheppard Regulatory Director, OCRSS.
Updates Personnel Updates: – Joseph Smallberger joins the team as our new eRA Technical Manager. – We are still looking for our Proposal.
Introduces ePIRATE electronic Portal for Institutional Research at ECU East Carolina University Office for Human Research Integrity.
Business Operations Pre-Award. What is required to begin the business process? Possible indicators CDA executed Cancer Center MDG/PRC approvals Department.
Research Orientation to SCCA. What is the SCCA? The SCCA brings together the outstanding adult and pediatric oncology patient care services of three world-
Getting a study done at Jefferson:. Startup Activities: Image courtesy of CITI Program Clinical Research Coordinator course.
A Road Map to Clinical Research at Jefferson. Required Training; prior to research activities: CITI Training COI (Conflict of Interest) eMR systems TJU/TJUH.
Stanley Estime, MSCI October 19, 2015 Record Keeping: What is Regulatory Documentation and how should it be maintained? Tel:
Updates in Research Protections Karen Allen Director, Research Protections Office of Research November
Research Review Application Process. Required research approval All MSA 699 students are required to obtain research approval prior to collecting data.
Conducting Research at Lincoln IRB/HRPP Policies, Procedures & Good Clinical Practices B Kanna MD, MPH, FACP Associate Program Director of Internal Medicine.
Clinical Research Coordinator Fundamentals Course Remuneration (Clincard) Laura Vinci, RN, MBA Senior Director of Operations Jefferson Clinical Research.
The TJU Human Research Protection Program (HRPP): Part I – Which Entities/Offices are Involved ? J. Bruce Smith, MD, CIP.
Non-compliance with Human Subjects Research Regulations J. Bruce Smith, MD, CIP November 2014 Continuing Education for IRB Members.
May 5, 2016 Working With CTO Contracting: How Do I Get My Clinical Trial Contract Negotiated & Why Isn’t It Signed Yet? Jaci Brown, Manager, CTO-Contracting.
Business Operations Pre-Award. Confidential Disclosure Agreements (CDA)/ Non-Disclosure Agreements (NDA)
A Road Map to Clinical Research at Jefferson. Required Training; prior to research activities: CITI Training COI (Conflict of Interest) eMR systems TJU/TJUH.
Lifespan 1 Submission Process to the IRB part 2 Revisions to Protocol.
Office of Human Research (OHR) Quality Improvement Program Patrick Herbison Heather Krupinski.
IRB BASICS BETTY WILSON, MS, CIP. CONCEPTS SUBMISSION APPROVAL RECRUITING WORKING WITH PRINCIPAL INVESTIGATOR (PI) /SPONSOR POLICIES DEVIATIONS RECORD.
Submitting to a Commercial IRB Kyle Conner, MA, CIP Associate Director Office of Human Research.
Research Review Application Process
Research Billing Compliance University of Iowa Health Care
Conditional IRB Approval
Research with Children’s Healthcare of Atlanta
Study Feasibility and Start-up
Completing Organization Approval
Investigator of Record – Definition
To start the presentation, click on this button in the lower right corner of your screen. The presentation will begin after the screen changes and you.
Getting Started with the Grants Portal Non-Grants
ESTR Basics for View-Only Users
Clinical Investigations
Sponsor Expectations for Clinical Studies
Multisite Human Subjects Research
Click Training Agreements Module
Electronic Submission to the Jefferson IRB Using the Portal
Basic iRIS Features and Submissions
Investigator of Record – Definition
Investigator of Record – Definition
Research Billing Compliance University of Iowa Health Care
UW-Madison Central IRB Gateway
Michael Linke, PhD, CIP Professor Department of Internal Medicine
Change to Commercial IRB Fees
Changes to the Common Rule and Single IRB (sIRB)
Research Billing Compliance University of Iowa Health Care
Research Billing Compliance University of Iowa Health Care
CTSA27 So you want COMIRB to be your sIRB: What you need to know.
Research Billing Compliance University of Iowa Health Care
Research Billing Compliance University of Iowa Health Care
Sleep SMART Clinical Trial Agreements / Regulatory Webinar
Michael Linke, PhD, CIP Professor Department of Internal Medicine
Presentation transcript:

Using A Central IRB At Thomas Jefferson University / Hospital Roseann Talarico Associate Director Office of Human Research

Joining an Existing Study with Quorum and WIRB Review IRB

 Complete ePTF and notify ORA of intention to join a study approved by Quorum or WIRB  Follow the standard process for creating a new study record in JeffTrial

 In the Portal, at the ‘Create an IRB Application’ drop-down menu, select ‘Quorum or WIRB’, and upload an OHR-1. (Be sure to check off ‘Quorum Review IRB or Western IRB (WIRB)’ at the top of the OHR-1.) This is the only document you will upload in the Portal. There is no paper submission.  If OHR authorizes the submission to proceed, it will issue a signed TJU-Quorum Institutional Cover Page or WIRB Cover Page.

Screening Criteria for Jefferson Investigators Applying to Commercial IRBs

The Office of Human Research will apply the following criteria when determining whether an investigator may apply to join a study approved by a commercial IRB: 1. Study is a phase 2, 3, or 4 multi- center, commercially sponsored clinical trial. 2. PI is in good standing with institution in regards to human subjects research compliance (e.g., PI is not currently on probation for violations). 3. PI & research staff have completed appropriate CITI training and are up to date with COI disclosures.

4. OHR-1 includes all required signatures. 5. PI has history of sound ethical judgment and the ability to manage clinical trials. 6.PI does not have a financial COI with the sponsor of the clinical trial. 7.Submit through JeffTrial and upload to the Portal.