A Federal Perspective on Compliance Division of Grants Compliance and Oversight Office of Policy for Extramural Research Administration, OER National.

Slides:



Advertisements
Similar presentations
MONITORING OF SUBGRANTEES
Advertisements

WHAT TO EXPECT IN AN EXTERNAL AUDIT OR INVESTIGATION An Overview of External Audit and Investigative Processes Performed by Outside Entities at UCSD.
Internal Controls What Are They And Why Should I Care? 1.
Yvonne Lau, MD, PhD, MBHL NIH Extramural Research Integrity Officer OD/OER/OEP National Institutes of Health OER Regional, June 2013.
Contractor Code of Business Ethics and Conduct Laura K. Kennedy Senior Vice President, Ethics and Compliance SAIC.
Presented by: Maritza Zeiberg, CPA,
MODULE 8 MONITORING INDIANA HPRP Training 1. Role of Independent Financial Monitors 2 IHCDA is retaining an independent accounting firm to monitor its.
Environmental Management Systems An Overview With Practical Applications.
Post Approval Monitoring Program Presented by Carolyn Malinowski Manager, Quality Assurance and Training.
Office of Inspector General (OIG) Internal Audit
Supplier Ethics: Program Checklist
Office of Research Integrity Office of Research Integrity Orientation Session November 8, 2012 ECSS
Effort Reporting: A Departmental Approach to Meeting Audit Requirements Dianne Valdez, MBA, CIA, CISA, CCSA Enrique Valdez Jr., MBA.
SAS 112: The New Auditing Standard Jim Corkill Controller Accounting Services & Controls.
Promoting Objectivity in Research by Managing, Reducing, or Eliminating Conflicts of Interest UT HOP UT HOP The University of Texas at Austin.
1 Susan Weigert, Project Officer GSEGs Overview of GSEG Management.
Control environment and control activities. Day II Session III and IV.
MANAGING THE SUBMISSION AND AWARD PROCESS Office of Sponsored Projects Main Campus and Branches.
Federalwide Assurance Presentation for IRB Members.
Foundation Financial Services Post Award Nancy Gomez Post Award Analyst.
Minnesota’s Internal Control Initiative National Association of State Comptrollers March 25, 2011 Speaker Jeanine Kuwik, MBA, CPA, CISA Director of Internal.
Central Piedmont Community College Internal Audit.
Audit and Fiscal Oversight Responsibilities VAVRINEK, TRINE, DAY & CO., LLP December 15,2010.
Research Conflicts of Interest: Identifying and Minimizing COI from the Perspectives of Sponsors, Faculty and the IRB Research Conflicts of Interest: Identifying.
Segregation of Duties– Sponsored Programs APM
1 INTERNAL CONTROLS Matthew Pakos School Improvement Grant Programs May 23, 2011.
CORPORATE COMPLIANCE Tim Timmons Vice President Compliance and Regulatory Services Health Future, LLC.
Effective Management and Compliance 1 ANA GRANTEE MEETING  FEBRUARY 5, 2015.
MANAGING SPONSORED PROJECTS FINANCIAL COMPLIANCE May 1, 2008 Office of Grants &Contracts Accounting.
Policy Council and Program Planning. The Head Start Program Planning Cycle National Center on Program Management and Fiscal Operations (PMFO)
Institutional Research Compliance Juliann Tenney, JD Research Compliance and Privacy Officer Director, Institutional Research Compliance Program.
Compliance Perspectives SRA 2002 Annual Meeting Orlando, Florida October 29, 2002.
AUDITS What you should know - a campus perspective. Franz Lozano Director/Budget Officer (former Internal Auditor) San Francisco State University Academic.
BTOP OVERSIGHT WASHINGTON D.C. MAY 2012 U.S. DOC Inspector General Recovery Act Oversight Task Force 1.
DCB New Grantee Workshop: Post-Award Administration of Grants Brett Hodgkins Team Leader National Cancer Institute Office of Grants Administration.
Got the Grant What’s next??????????? Joy R. Knipple Team Leader, National Institute of Mental Health July 26, 2006.
1 The Auditor’s Perspective Division of Sponsored Research Research Administration Training Series Presented by: Joe Cannella Audit Manager,
Important acronyms AO = authorizing official ISO = information system owner CA = certification agent.
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.
Best Practices: Financial Resource Management February 2011.
Office of the Vice Chancellor for Research 1 Update on PHS New Rule on Financial Conflicts of Interest (FCOI) Presentation to Business Managers January.
Managing Your Grant Award August 23, 2012 Janet Stoeckert Director, Research Administration Sr. Administrator, Basic Sciences Keck School of Medicine 1.
SBIR Budgeting Leanne Robey Chief, Special Reviews Branch, NIH.
10/16/2015 Roles and Responsibilities of Principal Investigators/ Program Directors/ Project Directors.
DCB New Grantee Workshop: Post-Award Administration of Grants Brett Hodgkins Team Leader National Cancer Institute Office of Grants Administration.
Research Compliance: An Overview of the Players and Issues Involved in Emory’s Research Compliance Programs.
1 Investigating Fraud & Abuse Violations in Medical Research Janet Rehnquist, Esq. Venable LLP th Street, NW Washington, DC
The Basics of the Effort Certification and Reporting Technology (ECRT) System.
1 101 on NIH Grants Understanding the Roles of VMRF and the Principal Investigator When Administering NIH Grants Last updated: December 2006 Veterans Medical.
1 QEM/BIO Workshop October 21, 2005 Award Administration.
Debra Murray, Georgetown University Tolise Miles, Children’s National Medical Center Clairice Lloyd, Georgetown University Medical Center Pre-Award and.
Roadmap For An Effective Compliance And Ethics Program The Top Ten Things the Board Must Know [Name of Presenter] [Title] [Date]
DCB New Grantee Workshop: Post-Award Administration of Grants Brett Hodgkins Team Leader National Cancer Institute Office of Grants Administration.
Animals in Research: Navigating the Animal Protocol Approval Process Summer Seminar Series Susan Warren IACUC Chair.
Daily Management of Awards Jennifer Crockett Jennifer Crockett, Director, Sponsored Projects Finance, Columbia University Tamara Hill Tamara Hill, Manager,
University of Minnesota Internal\External Sales “The Internal Sales Review Process” An Overview of What Happens During the Review.
A Guide for Management. Overview Benefits of entity-level controls Nature of entity-level controls Types of entity-level controls, control objectives,
MICHELLE BULLS DIRECTOR, OFFICE OF POLICY FOR EXTRAMURAL RESEARCH ADMINISTRATION.
“SPEAR” W ORKSHOP O CTOBER 19 & 30, 2015 ANGELLE GOMEZ S UBAWARD R ISK A SSESSMENT / MONITORING.
Indian Health Service Grants Management Grants 101- Fundamentals.
Lifecycle of an Award Reporting, Close-outs and Audits Michelle Vazin, Vanderbilt University Michele Codd, George Washington University.
Internal Audit Section. Authorized in Section , Florida Statutes Section , Florida Statutes (F.S.), authorizes the Inspector General to review.
Jaimie Lewis Omnitrans San Bernardino, California SUBRECIPIENT MONITORING.
Important acronyms AO = authorizing official ISO = information system owner CA = certification agent.
What’s your friend up to? Subrecipient Monitoring Issues Tom Egan, MIT OSP Jeannette Gordon, Division of Grants Compliance and Oversight OPERA, OER, NIH.
AISL PI Conference February 29, 2016 Division of Grants and Agreements.
New Faculty Orientation
The Process for Final Approval: Ongoing Monitoring
Centralization of Texas State Contract Compliance Functions
Uniform Guidance and Grants Accounting
Presentation transcript:

A Federal Perspective on Compliance Division of Grants Compliance and Oversight Office of Policy for Extramural Research Administration, OER National Institutes of Health, DHHS

Division of Grants Compliance and Oversight Director OPERA Director, Division of Grants Compliance and Oversight Assistant Grants Compliance Officers This Division was established on August 28, 2001 and has the responsibility for managing both internal and external compliance activities.

NIH Objective To ensure continued progress on current and future NIH-supported research activities while minimizing risks to Federal funds

Research is a Partnership Collaborative relationship between NIH and grantee Mutual need to assure compliance and implement proactive compliance measures

Who is Responsible? At NIH Grants Management Officer/Specialist Program Official Scientific Review Administrator At the institution Authorized Organizational Official Principal Investigator

Compliance Begins at Home You must be in compliance with institutional as well as Federal requirements When you have a policy or procedural question, start at your institution - institutional requirements may be more restrictive Read the Notice of Award

A Few Ground Rules Grant awards are made to institutions Recipients of NIH grant funds must comply with all applicable Federal statutes, regulations, and policies By drawing funds from the HHS Payment Management System, grantees agree to the terms and conditions of the grant award

Common Contributors to Compliance Problems Inadequate resources Lack of understanding of roles and responsibilities of institutional staff Inadequate staff training and education Outdated or nonexistent policies and procedures Inadequate management systems (e.g., effort reporting, financial management) Perception that internal control systems are not necessary

Roles and Responsibilities Roles and responsibilities should be clearly defined, communicated, and accessible

Establish Roles and Responsibilities Provide a detailed listing of responsibilities, including oversight responsibilities, by role Communication is essential. Foster working groups or discussion groups for staff involved with grant and contract administration at the sponsored research and departmental levels Ensure there is a connection between these groups, so key information, policy changes, and new developments are consistently communicated

Establish Roles and Responsibilities Provide links to related resource information, such as institutional requirements, policies and procedures, cognizant offices, subject matter experts, contact information, and training and education opportunities Establish a compliance officer position and/or office or committee

Training and Education Programs A culture of compliance begins with a culture of understanding

Develop Effective Training and Education Programs Training and continuing education is critical! Develop formalized education programs and consider mandatory training requirements Offer certificate programs Involve respected faculty members to promote faculty buy-in

Develop Effective Training and Education Programs Utilize individual training plans Roles and responsibilities Internal audit findings are future training opportunities Designate a central source of information Education Coordinator/Office that oversees all training programs and evaluates them for content and effectiveness

Develop Effective Training and Education Programs Develop an education program to accommodate new and existing staff Orientation for new employees Continuing education programs for staff involved with sponsored research Include all personnel with a role in sponsored research, including PIs, departmental administrators, and sponsored programs staff

More on Training and Education – Training Tips Keep sessions short and provide incentives (e.g., food!) Provide training locations both on and off campus (accommodate your busy research staff by bringing the training to the labs) Supplement training with web- based information and resources, such as online training modules

More on Training and Education – Training Tips Training must be kept current and should be consistently provided, otherwise staff may not view it as significant Use case studies – they are an effective way to stimulate rich discussion Include a mechanism for feedback to improve course content

Policies and Procedures Accessibility of written institutional policies and procedures is vital

Maintain Current Written Policies and Procedures Accessibility of written institutional policies and procedures is vital Maintain centrally Use plain language Update/review regularly to ensure reliability Include roles and responsibilities Make widely available online Provide contact for questions and updates

Maintain Current Written Policies and Procedures Assign oversight responsibilities Responsibility = authority Develop policies with input from involved staff Utilize internal audit findings when developing policies and procedures Develop procedures that will set a consistent standard

Management Systems Grantee organizations are expected to have systems, policies, and procedures in place by which they manage funds and activities

Effective Management Systems Effective management systems include: Clear delineation of roles and responsibilities Written policies and procedures Training Internal controls Effective oversight Information sharing Systems must provide reliable and current information Management systems should be driven by policy vs. process

Examples of How to Improve Oversight (Financial Management) Sponsored programs (pre/post) should be more actively involved in financial oversight Perform spot checks of areas in which there are repeated findings or repeated questions Perform a random review of selected categories of transactions on every grant at closeout Utilize internal audit findings to improve systems Review cost transfer policies to ensure requirements for making appropriate cost transfers are clear and correct. This area is often misunderstood by institutional officials, PIs, and departmental administrators

Examples of How to Improve Oversight (Financial Management) Provide the PI with a summary of the terms and conditions of each grant award Require PIs to certify that they have reviewed monthly expenditure reports and agree with charges to their projects Send notification to PI ninety days prior to end of a project period informing him/her that the project is about to end, work must be completed, and all transactions processed in order for final reports to be prepared and submitted to the sponsor in a timely manner Provide FSRs to PIs, either before or after submission, to have them verify the accuracy of the information submitted to sponsors

Strengthen Internal Control Systems Management tools to help achieve results and safeguard integrity Provide reasonable assurance Promote efficiency and effectiveness Encourage compliance Ensure that internal controls are functioning as intended to achieve objectives Utilize Internal Audit – independent evaluation Perform risk assessments –focus on high risk events

Examples of Internal Control Activities Written policies/procedures Segregation of duties Approval and authorization Verification Physical restrictions Documentation Monitoring and reporting

What We Have Learned An effective culture of compliance must be established from the TOP and be an institutional expectation Establish a mechanism for concerns to be heard Personnel need to understand their responsibilities

What We Have Learned Training and education are critical Good communication throughout the institution is essential Adequate systems must be in place to support an effective compliance program Don’t wait for a catastrophe to start thinking about compliance – take a proactive stand

NIH Proactive Compliance Site Visit Initiative Proactive Compliance Site Visits Division of Grants Compliance and Oversight, OPERA, OER, NIH Not an audit or investigation No report Mutual information exchange – emphasis on partnership

NIH Proactive Compliance Site Visit Program has… Supported the NIH goal of moving from reactive to proactive interactions with our recipient community and demonstrated that: Compliance is an ongoing and dynamic process that is more likely to be present and effective if it is established as an institutional expectation Proactive visits confirm and expand the foundation of partnership between NIH & the recipient Proactive visits encourage and support recipient efforts to effectively administer and improve sponsored program activities

Proactive Compliance Site Visit Summary: FY2000-FY institutions Top 150 NIH-supported institutions 20 universities/medical schools 4 nonprofits (3 AIRI institutions) 2 hospitals Geographic diversity Expanded education-outreach seminar Proactive Compliance Site Visits: A Compendium

Dear Grants Compliance… Q - What does it mean to be designated a “High Risk” grantee by the NIH and what actions are taken against the grantee? A – The NIH Grants Policy Statement has a section on “Enforcement Actions” There is not a predetermined set of special terms and conditions imposed if a grantee is designated as high risk. Actions to increase NIH oversight such as removal of Expanded Authorities and exclusion from the “Streamlined Noncompeting Award Process” have been used in the past, but each case is reviewed and actions taken based upon the specific circumstances involved.

Dear Grants Compliance Q – How do I report scientific misconduct related to NIH grants? A – You should notify the Office of Research Integrity (ORI), Department of Health and Human Services, of scientific misconduct involving: (1) research supported by Public Health Service (PHS) funds; or (2) an application for PHS funds. The National Institutes of Health (NIH) as well as several other agencies are a part of the PHS. The following ORI website provides further information about reporting scientific misconduct ( ).

Dear Grants Compliance Q - I suspect grant funds are being inappropriately spent and would like to speak to someone to report misuse of NIH grant funds. Who should I contact? A - You have several options for reporting financial mismanagement. If you would like to gain further insight into the situation or discuss institutional policies, you may want to begin by contacting the grantee institution (Sponsored Research Office) or the NIH grants management office that funded the grant:

Dear Grants Compliance (cont’d) If you would like to make a formal allegation of misuse of grant funds, you should contact either of the following two organizations with your complaint. You may submit an anonymous complaint if you so choose. NIH Office of Management Assessment Division of Program Integrity Phone: (301) Fax: (301) DHHS Office of Inspector General: Phone: HHS-TIPS ( ) (this is a Hotline number which offers a confidential means of reporting allegations)

Dear Grants Compliance Q – Can I submit an application to different institutes within the NIH, or to AHRQ, at the same time? A - Submission of more than one application within the same review cycle is permissible for some, but not all, award mechanisms: For a NRSA Fellowship (F series), only one application may be submitted in the same review cycle. For an investigator-initiated grant (R01), small grant (R03), career development award (K-Series, excepting K08), small business innovation research grant (SBIR), small business technology transfer grant (STTR), or a conference grant (R13), more than one application in the same review cycle may be submitted, if each application describes a different research topic…

Dear Grants Compliance (cont’d) …Submissions of identical applications to different agencies within the PHS or to different Institutes within an agency are not allowed. Essentially identical applications will not be reviewed except for: 1) an application for an independent Scientist Award (K02) proposing essentially identical research in an application for an individual research project; and 2) an individual research project identical to a subproject that is part of a program project (P01) or other P-series grants, such as P30 or P50.

Useful Websites NIH Guide for Grants and Contracts Grants Policy and Guidance Proactive Compliance Site Visits FY2000-FY2002: A Compendium of Findings & Observations compendium_2002.htm NIH Conflict of Interest Information

Useful Websites Office of Management Assessment Office of the Inspector General Office of Research Integrity Office for Human Research Protections Office of Laboratory Animal Welfare

Questions?