Now that your institution has been awarded the funds required to carry out your research project, it is only a matter of time before the agreed upon terms and conditions between you and the regulatory entities demand more and more of your attention.
In order to successfully comply with the regulatory requirements of multiple state and federal agencies, institutions must build strong internal auditing and monitoring programs. Failure to do so could put you at risk of serious compliance violations, or grant fraud scenarios, such as these:
- Columbia University settles False Claims Act allegations involving mismanagement of federal grant money, which included failure to accurately monitor and track the employees' work hours which were reported to grant fund managers for reimbursement. The total settlement amount was $9,020,073.
- The University of California Davis agrees to pay $499,700 to resolve allegations of federal grant fraud involving failure to disclose overlapping and duplicative awards of grant money.
To protect yourself, the research and your institution, developing a robust auditing and monitoring program that will identify and correct non-compliance proactively is KEY.In this 60-minute online training, Ms. Charboneau Wishon will cover the following topics:
- More quickly correct compliance issues with regulatory and accrediting standards
- Easy-to-implement audit guides to help prepare you for an audit
- Pin down the most common sponsor requirements
- Incorporate essential elements into your corrective action plan
- Develop and implement an economical compliance monitoring plan
- Improve your research team’s knowledge of regulatory requirements
- Upgrade regulatory and auditing training with limited resources at research sites
- Avoid increased diversions from your research to deal with regulations
Who Should View? Any and all research staff members involved in research policy, regulation and compliance will benefit from this training. This can include research faculty, research office staff, lab members, administrative staff, research and compliance team members, and research site monitors.By implementing the strategies presented in this online training, you will be able to effectively evaluate either a single research project or your institution’s entire portfolio for regulatory compliance violations, as well as develop a corrective action plan that works. So, don’t wait, register today.
Register for this, must-watch grant writing session for only $167 (regular list price $197). Save $30 instantly.
Meet Your Expert: Angela R. Charboneau Wishon, JD
Ms. Charboneau Wishon most recently served as the Vice President for Research Administration at the University of Texas Southwestern Medical Center where she had regulatory responsibilities for the research compliance programs, including the Human Research Protections Program, and the Research Compliance Committee. Prior to joining UT Southwestern, Angela served as the Assistant Vice Chancellor for Regulatory Compliance at The University of Colorado Denver, coordinating the compliance programs on the UC Denver campuses. Additionally, she served as the Director of the Regulatory Knowledge and Support Core under the Colorado Clinical and Translational Sciences Institute. She serves as site visitor for the Association for the Accreditation of Human Research Protections Program (AAHRPP) and is an active member of the National Council of University Research Administrators (NCURA), where she is a member of the Professional Development Committee, a co-editor for NCURA Magazine, and a past faculty member of NCURA Sponsored Programs II course.
Angela is an active member of several professional associations, including the Society of Research Administrators International, Association of Clinical Research Professionals, and Public Responsibility in Medicine and Research. She has served as a co-investigator on multiple NIH awards in the areas of regulatory affairs and ethics and has spoken on the topics of Research Compliance Programs, Research Audit Management, Conflict of Interest Issues, Human Subjects Protections, and Monitoring Plans at various state and national meetings. Furthermore, she has co-published an article titled: “A Tricky Business: Assessing Risks from an Institutional Perspective,” Clinical Researcher, Cheryl Chanaud, Ph.D., Ann Smith and Angela Wishon, J.D., February 2001.
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How do PI Leader Online Training Sessions Work?
PI Leader sessions provide you with best-in-class expert education and advice to address all of your non-science needs such as grants and funding, lab management, intellectual property, lab animal welfare and many other topics. Our online training (Live or On-Demand) are a cost-effective and convenient way to boost your chances for more funding and lab/research productivity. You can participate in the comfort of your office without incurring travel costs and time.
You have 3 training options depending on your needs that you would select by a drop-down menu after clicking the order now button below:
- ON-DEMAND: This format allows you to access a live recording of the training session. You get the exact same training, Q&A and handouts as the live session, but can listen to it at your convenience.
- CD: The exact same training and handouts are saved on a CD and mailed to you. It takes a little longer, but gives you a little more flexibility.
- TRANSCRIPT: The expert speaker's words are transcribed into a document and sent to you by email. It takes up to 10 days, but allows you to read the content.
With every option, your registration includes learning aids such as presentation handouts and other helpful materials.
PI Leader also offers site licenses and additional connections for your group or institution at discounted prices.