All forms can be viewed and printed as PDF documents (Adobe Acrobat Reader required).
If you need help completing forms contact the Office of Sponsored Research Administration (OSRA).
Downloads and Links
|Form name||Description||Download Link|
|Adobe Forms D (NIH) – WCM Template||The Adobe Forms D package is to be used for due dates on or after May 25, 2016. This template is provided for reference purposes only, and is not intended to be completed for submission to NIH. For up-to-date application packages, visit the NIH website: http://grants.nih.gov/funding/index.htm and search for the appropriate Parent Announcement or RFA.||Adobe PDF|
|Addendum to Outside Consulting Agreement||Outside Consulting Agreements are considered to be personal arrangements between the WCM faculty member and the Company. WCM University Counsel requires this non-negotiable Addendum be signed by the Company and incorporated into the faculty member’s Outside Consulting Agreement.||Microsoft Word|
|Advance Account Request Form||As described in the form, this is for new and competing grants where WCM is prime and award notice is pending release from the Sponsor or processing is otherwise delayed. Submit request to initiate the set-up of a new account in order to commence work and allocate expenditures appropriately.||Adobe PDF|
|Annual Compliance Checklist||Adobe PDF|
|Budget Template - OSRA|
OSRA's Standard Budget Template establishes a uniform model for use across all sponsored research funding. Use of this template will greatly assist OSRA as they review budgets and create accounts in SAP.
|Carryover Request Template Letter||Microsoft Word|
|Certificate of Registration for Use of Recombinant DNA or Transgenic Animals||Microsoft Word|
Template A: Outside Entity to Faculty/Investigator CDA
Template B: Cornell to Outside Entity CDA
|Template A: This template should be used when the sponsor of a potential study is providing confidential information to a WCM scientist/investigator. |
Template B: This is template should be used when a WCM scientist/investigator is providing confidential information to a potential sponsor.
|Consulting Agreement Template|
A consulting agreement is required for consulting services budgeted on a sponsored project. The attached agreement is a non-negotiable template to be signed by individuals outside WCM with the role of consultant on a funded sponsored project.
|Cost Sharing Form||If institutional or Departmental funds will be used to support a portion of this project, please explain on the Cost Sharing Form.||Adobe PDF|
|DHHS Rate Agreement||Adobe PDF|
|Dissemination Plan Template||This template should be used by investigators submitting a human subjects/clinical trial proposal to NIH using Forms E.||Microsoft Word|
|Effort Reduction Template||For all grants where an effort reduction approval is being requested from the Sponsor. For NIH, effort reductions greater than 25% should be submitted for key personnel named in the Notice of Award. For subawards and other Sponsors, follow the prime/sponsor agreement or notice of award guidelines.||Microsoft Word|
|Equipment Survey Form||On a proposed sponsored project, complete this form for each proposed equipment purchase costing $5,000 or more. The Equipment Survey Form allows the Institution to confirm that the equipment is not already available on Campus.||Adobe PDF|
|Export Controls Checklist||"Export Controls" are those federal laws and regulations that govern the transfer or disclosure of goods, technology, software, services, and funds to restricted foreign countries, persons and entities (including universities). Your response to the questions in this checklist will help the Grants & Contracts Office and the Office of University Counsel determine whether any aspect of your sponsored research project activities will be subject to export control regulations.||Adobe PDF|
|Foreign Exchange Risk Acceptance||Adobe PDF|
|Grant Transfer Checklist for PI Transferring FROM WCM to NEW INSTITUTION||This form should be completed by the Weill-Cornell Principal Investigator leaving WCM that wishes to transfer his/her grant(s) and/or contract(s) from WCM to another organization when allowed by sponsor policy.||Microsoft Word|
|Grant Transfer Checklist for PI Transferring TO WCM from FORMER INSTITUTION||This form should be completed by the new Weill-Cornell Principal Investigator transferring his/her grant(s) and contract(s) to WCM from another institution.||Microsoft Word|
|Guidance for Conflicts Disclosure||Adobe PDF|
|Hospital Facilities Form||If a sponsored research project will be using any New York Presbyterian Hospital Facilities (space, ancillaries, personnel, data or information systems), a Principal Investigator must detail this use on the Hospital Facilities form.||Adobe PDF|
|Human Research Billing Analysis Form||Principal Investigators are required to submit one Human Research Billing Analysis Form per research protocol at the time of the IRB submission application for new protocols and again at the time of continuing review. The purpose of completing and submitting a Human Research Billing Analysis Form is to prospectively identify the list of services required by the study protocol, and indicate when the services will occur, who will provide the service, how the service is to be billed and in general terms, specify payment responsibility.||Microsoft Excel|
|Human Subjects Protection Training Verification Form||The Human Subjects Protection Training form is completed to confirm that all WCM key personnel listed on a sponsored research project have completed the CITI "Biomedical Research Investigators and Key Personnel Course" web-based training.||Adobe PDF|
|Laboratory Safety Registration (replaces Research Safety Checklist / IBC Registration)||The "Research Safety Checklist/IBC Registration" and "Research Safety Checklist/IBC Registration - Short Form" have been replaced by the "Laboratory Safety Registration". Submit the Laboratory Safety Registration where prompted to upload the "Research Safety Checklist/IBC Registration". Environmental Health and Safety will assist researchers with obtaining your required IBC approvals for all of your laboratory's rDNA and biohazard work; Radiation Safety Committee approvals for all radioactive non-human use work; and the Research Safety Checklist for safety program implementation within the laboratory. Follow the link on the right to download the "Laboratory Safety Registration," follow all form instructions, and contact EHS at email@example.com or (646) 962-7233 with questions about the form.||Adobe PDF|
|Material Transfer Agreement (MTA) - Simple Letter Agreement (SLA)||Microsoft Word|
|No Cost Extension Template||Microsoft Word|
|No Cost Extension Template (Non-Federal Sponsors)||Microsoft Word|
|Pre-Award Costs Request Template||For new, competing and non-competing grants for which a notice of award has been received with a later than anticipated start date and allowable pre-award costs is being requested.||Microsoft Word|
|Request for Reduction in Indirect Costs||For any instance where a sponsored research project does not provide an approved indirect cost rate, please complete this waiver request.||Adobe PDF|
|Scope of Work Form|
If a sponsored research project’s scope of work will involve any existing intellectual property and/or is likely to generate intellectual property, please indicate the details on the Scope of Work form. This form should not be used for subawards and consortiums where a scope of work is required.
|Statement of Intent to Establish a Consortium Agreement||A statement of intent form is required for all subcontract sites participating on a WCM grant application. Please have the form completed and signed by your collaborator's central business office.||Adobe PDF|
|W-9 Form||Adobe PDF|
|WBS Element Request Form||The purpose of this form is to ensure that all WBS elements (for new, competing and supplemental applications) are created with the appropriate levels of SAP access.||Adobe PDF|