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Care New England Research

Manage an Award

Now that you’ve been awarded funding and your project is up and running, you’re in the post-award phase. Below you will find information applicable to many award types across CNE Research from charging expenses to awards to completing annual reports. However, each award is guided by specific terms and conditions found in the notice of award. Make sure you read yours carefully and understand any restrictions or special conditions that may be in place. 

Effort Compliance

PIs and Key Personnel must certify their effort on a monthly basis. For questions contact your Post-Award Specialist.

Managing Expenses

Project expenses can be viewed on Tableau. Expenses, excluding salaries, are updated continuously. Salaries are updated as soon as the prior months’ financials close

 

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Charging Expenses
to a Grant

PIs have a fiduciary responsibility to ensure all expenses on their projects are allowable, allocable, and reasonable and meet the terms and conditions of the award or contract. This includes expenses budgeted and invoiced by sub-recipients on the award.

Purchasing: Remember to contact Purchasing with questions or concerns before placing an order. 

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Activity String

**Beginning in mid-2022 activity numbers will not change each project year for all newly set-up accounts. Activities will be used for the life of the project, until competitive renewal.

Company
1000 for CNE, 2110 for Butler, 2310 for WIH, 2210 for Kent, etc.
Subaccounts
Accounting Unit
Activity Number

Biospecimens

Human Biospecimens

Biospecimens are sample materials taken from the human body such as blood, urine, tissue, and other body fluids or materials obtained from humans.

Ethical Considerations

Activities involving the use of biospecimens for research meet the definition of human subjects research and therefore must comply with the activities described in the informed consent signed by the participant or under a waiver of consent granted by an IRB in accordance with 45 CFR 46.

Requirements for Working with Human Specimens

All CNE employees provide immunization records or are screened for immunity during their CNE Occupational Health New Hire Appointment. Vaccinations that are recommended, but not required (such as Hep B) are offered to the employee.

Collection and Storage

Biospecimens that are collected and stored for research purposes must be handled in accordance with the U.S. Occupational Safety and Health Administration’s Bloodborne Pathogens Standard. Research teams should develop a Standard Operating Procedure (SOP) for the collection, labeling, storage, and retrieval of biospecimens. The SOP must describe procedures appropriate for the type of biospecimen being collected. Additional regulations apply to biospecimens classified as select agents or toxins (42 CFR 73).

Packaging and Shipment

Packaging and shipment of human biospecimens and other dangerous goods (including dry ice) must conform to all applicable regulations, including but not limited to the U.S. Department of Transportation and International Air Transport Association guidelines. Any individual involved in the shipment of biospecimens must be properly trained. Training can be obtained from the following sources:

IATA

Infectious Substances Shipping Guidelines Course

Saf-T-Pak

Shipping Infectious Substances and Related Materials, incl. Category A (UN2900, UN2814 UN3373) Online Training Course

Shipping Category B Biological Substance and Related Materials (UN3373) Online Training Course

NIH Prior Approval Requests

The activities below require prior approval from NIH.

Information required for all request types:
  • PI Name
  • Grant Title & Grant Number
  • Name and email address of NIH grant officer (if possible)
No-Cost Extension Requests
Change in PI/Key Personnel Requests
Rebudgeting Requests
Change of institution request
Carryover Requests
Change in Scope Requests
Requesting a New Subaward
Requesting a Significant Change in Effort (>25% change in effort)

NIH RPPR

The Research Performance Progress Report (RPPR) is used by grantees to submit annual or other interim progress performance reports, as well as final progress, reports. The terms and conditions of the award will provide guidance on the frequency of performance reporting required. Annual RPPRs typically report scientific progress, identify significant changes, report on all project personnel, and plans for the next budget period. Late or missing progress reports can lead to delayed funding. 

Consider delegating the ASST role in eRA Commons to someone who can help initiate or complete the RPPR in eRA Commons.

Information to complete the RPPR:
  • Basic institutional and project information
  • Accomplishments from the past activity period and goals for the upcoming period
  • Products from the prior activity such as technologies or publications
  • Effort of all personnel, including collaborators
  • Impact of the project and major contributions
  • Changes to the project, delays, changes in scope, other support, compliance, etc
  • Budget information (if applicable)
  • If Applicable, animal or human subjects enrollment information

Helpful Links

NIH RPPR: Who, What, When, Where, and How

eRA Commons Help: RPPR Module

Human Subjects Submission Process

Human Subjects System (HSS) Training Resources

RPPR FAQ

Foundation/Contract/Industry Sponsored Reports

Refer to the terms and conditions of your agreement to determine milestone and other reporting requirements.

FAQs

A piece of equipment I need to complete the aims of my NIH grant broke in the last year of funding. Can I use NIH funds to replace it?

No, major equipment cannot be purchased in the last year of a grant without permission. Contact your post award specialist to submit a request to your program officer.

What should be included on my other support pages?
What if I’m not sure if something should be included as other support?
I receive salary support from my RRF, does that need to be included on my other support?
What is “in-kind” support?
Where do I find a list of things that can and cannot be charged on an NIH grant?
Can I charge the cost of meals for lab meetings or quarterly research progress meetings with research staff?
How do I know if my award is SNAP eligible?
Who are considered key/senior personnel?
What does NIH review when it looks at other support submissions?
Is other support limited to grants where I receive direct salary support?
What does NIH mean by “foreign component”?
I conduct focus groups with research participants. Can I provide food?
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