Completing an RPPR can be a daunting challenge especially if one is new to the process. This session will go through an actual Progress Report (RPPR), section by section in detail explaining the requirements that NIH will review. The session will go over addressing the common errors and warnings and how to avoid the common pitfalls that result in a late submission or a non-compliant RPPR that can result in further inquiry from NIH. This session will go over the difference between SNAP and Non-SNAP RPPRs, Multiple component RPPRs, completion of the Budget Section H for applicable activity codes and dive into HSS/ASSIST for Human Subjects reporting requirements. Difference between Annual, Interim, and Final reports will also be discussed.

The term “Research Compliance” has become an integral part of research management vocabulary. Research compliance requirements cover a myriad of federal, state, local, and international regulatory and ethical rules and standards as well as institutional and funder policies that govern the entire life cycle of a research project. A successful compliance program is made stronger and more effective when the compliance requirements are seen as a “shared responsibility” where all individuals involved life cycle of a research project (i.e., the inception of the project; proposal preparation and submittal; acceptance and management of the awards; the conduct of the research and reporting of its finding; and close-out), clearly understand their role and the importance “doing the right thing” to ensure compliance with regulatory and ethical requirements seamlessly. To navigate this ever-changing environment, it is important for institutions to focus on developing a “culture of compliance” by creating an organizational environment where following regulatory and ethical obligations is a highly valued expectation. In this webinar we will discuss this concept in greater detail and discuss practical ideas on how to achieve a true “Culture of Compliance”.

The pandemic temporarily halted travel on sponsored awards, but now researchers are resuming their global journeys for the sake of research! Come and join us for a session on federal travel regulations, where we will cover the rules for Fly America, Open Skies, per diem, combining personal and business travel, and more!

Ever wondered what export controls are? Have you seen a grant or contract term referencing EAR, ITAR or OFAC and didn’t know what that meant? We (2 export control professionals) will give you the fundamentals and the tools to recognize export control concerns in the grants life cycle. We’ll explain the basics behind the regulations and walk through red flags that further analysis by a knowledgeable export controls resource is likely warranted. Lastly, the webinar will describe a few hypothetical case studies that we’ll break down.

In this webinar, participants will learn how to develop complex budgets for large research center projects. Topics covered will include a presentation on how different costs can be supported through campus-wide policy development and resource planning tools. The presentation will end with a deep dive by building a sponsor budget task-by-task and aligning that budget to schedule milestones and tasks.

Cost sharing can be an enigma to many new research administrators, and it can be a headache to many seasoned research administrators. What is it, is it really that daunting, and how can we turn this obligation into an opportunity? This presentation will help participants define cost sharing, identify the types of cost sharing, explain ways we can meet cost sharing requirements (including handling subs!), and touch on best practices and experiences from the presenter's time in research administration - including a discussion of understanding subrecipient cost sharing obligations.

Borrowing from this popular phrase with origins in Southeast Asia, this session will explore the similarities and differences between research administration offices of all sizes whether central or departmental. While our research volumes are drastically different, the workloads, per capita funding for staffing, and stressors are quite similar. Join us as we provide our perspectives from our different vantage points. We will discuss staffing challenges, remote/hybrid workforces, and dealing with last minute proposals along with the challenge of being all things to all people.

This session will provide a broad overview of the proposed NSPM-33 program requirements. We will discuss which requirements are least likely to change and which have the greatest potential to change before the final guidance is released. We will host a dialogue about what participants are doing at their own institutions to prepare and where they are holding off. Finally, we will offer some ideas for how to start or keep the conversation going at your home institution.

This webinar will explore the internal controls framework for subrecipient monitoring based on federal regulations. By close examination of the rules, this session will break down the requirements (must!") vs. the nice to haves ("should!") and how to create a compliant institutional framework.

Academic institutions are committed to maintaining openness and inclusivity in research, whether the collaboration is across campus, the region, or the globe. Institutions must uphold their missions while navigating a changing regulatory landscape and foster due diligence in international activities to mitigate risks and promote principled collaborations. This workshop will provide the latest information on NSPM-33 and relevant CHIPS Act research security requirements. It will offer attendees the opportunity to engage with each other on strategies for preparing for and implementing a research security program. University-wide awareness and engagement are critical for developing an effective program. Workshop leads will discuss how they have garnered institutional support for creating or updating university policy and processes in preparation for meeting NSPM-33 standards and elicit successful strategies from participants. Lastly, panelists and attendees will work in small groups and report out key strategic developments, investments, and resources that their respective universities have made.

This workshop provides a primary basis of understanding of proposals to and awards from the National Science Foundation (NSF). The program is perfect for someone new to research administration, as well as for research administrators seeking to expand their knowledge of federal funding agencies. The curriculum provides an overview of the policies and procedures essential to preparing successful proposals to and managing grant awards from NSF.

This workshop provides a primary basis of understanding of applications to and awards from the National Institutes of Health (NIH). This workshop will give you the basics and we will walk you through the grants process, and give you an overview of key resources and websites you will need to be successful. The program is perfect for someone new to Research Administration, as well as for Research Administrators seeking to expand their knowledge of NIH. The curriculum provides an overview of the policies and procedures essential to preparing successful applications to and managing grant awards from the NIH.