The Office of
104 Airport Drive Suite 2200, CB 1350
Chapel Hill, NC 27599-1350
Phone: (919) 966-3411
Fax: (919) 962-5011 or (919) 962-3352
Email: resadminosr@unc.edu
RAMSeS Help desk: (919) 843-2594
The PI is ultimately responsible for the proposal and corresponding activities including scientific, administrative, fiscal and ethical performance. Day-to-day financial management may be delegated to administrative staff, but accountability for compliance with University and Sponsor requirements ultimately rests with the PI. All proposals are subject to University review and oversight, in accordance with all relevant state and federal regulations, University policies and contractual obligations. If the project involves Co-Principal Investigators from different schools, each school should follow its own policies for determining who will act as lead investigator.
The PI eligibility page provides additional information about the roles and responsibilities of PIs at UNC-CH.
A Business Manager’s/Research Administrator's expertise and input is important in preparing a proposal’s budget and reviewing the funding agency's announcement for any special terms and conditions to assure that proposals are prepared accurately and completely. This person is also instrumental as an interface between PIs and OSR in assuring that completed proposals are routed through their Department and submitted to OSR in a timely fashion so that reviews and sponsor submission deadlines are met.
Typically, while constructing a proposal, the PI consults the department head or laboratory director regarding the availability and use of space and personnel and secures his/her approval. If the research involves human subjects, animal subjects, or hazardous substances, approval of the relevant committees should be obtained prior to submission to the Dean or his/her designee. If research involves investigators from more than one department/unit, one department is selected to administer the award (admin department), but each department/unit must still provide approval for the use of space, personnel, and/or equipment to be used on a particular project.
The Dean/Director/Chair of the lead unit reviews the application and agrees that the PI is appropriately qualified for performance of the project; that it is an appropriate activity within the Department/Center/Institute; and that the Department/Center/Institute has agreed to provide any resources identified in the application. When applicable, these resources could include cost sharing and the responsibility for reimbursement of costs to the University in the event that the sponsor is unable to pay the University for research expenses incurred during the period of performance of the project. In the event that signature authority has been delegated to another person for purposes of approving the Internal Processing Form, a copy of this delegation is kept on file in the department. However, ultimate responsibility for the Department/Center/Institute named on the application remains with the Dean/Director/Chair.
The Office of Sponsored Research (OSR) is required to evaluate all proposals, awards, agreements, or contracts prior to submission in order to certify that commitments made can be honored, and verify the accuracy of the information supplied. Each application is evaluated for compliance with University policies, agency guidelines, and where applicable federal regulations (i.e., animal use, human subjects, conflict of interest). OSR works in concert with departmental offices and central administration to prepare and submit the application. Under a specific delegation of authority from the Vice Chancellor for Research and Economic Development (VCRED), OSR has signatory authority to enter into legal commitments for the University for all proposals, grants, cooperative agreements, and contracts associated with research and training activities .
SPO signs for UNC-CH SOM on proposals to NIH (R, K & F Series) and American Heart Association(AHA) and American Cancer Association (ACA) typically, single investigator awards. (Link)
OCT negotiates and executes clinical trial agreements between the University and industry sponsored trials. OCT also processes clinical trial subcontracts, other types of agreements related to clinical research at UNC, and their associated IPFs. (Link)
General Guidelines
To assure that OSR properly executes the University's responsibilities with adequate time to provide investigators with appropriate feedback on their applications and to ensure timely submission to the funding agency, it is necessary that applications with published and/or established agency deadlines be received by OSR at least 5 business days prior to the due date. Proposals that have no established deadlines will be processed as soon as possible depending on the circumstances and the urgency.
Should there be any question regarding the routing of a proposal or contract for signature, contact the Director of Pre Award Services in OSR for guidance.
Specific Guidelines
JIT Information is provided at the request of the granting agency and as applicable, includes a request for the following documentation: Active/Pending Support for all Key Personnel named in the grant proposal; IRB Approval; IACUC Approval; Certification of Human Subjects Education** for Key Personnel. JIT request may also require other information such as a detailed budget and/or other information deemed necessary by the agency.
A signing official of the University must approve all JIT documentation prior to providing the information to the granting agency.
A cover letter to the agency should accompany the JIT documentation to the Office of Sponsored Research (OSR) or the Sponsored Programs Office (SPO) as applicable for SOM proposals, with the signature of the principal investigator and a countersignature line for Tony G. Waldrop, Ph.D., Vice Chancellor for Research and Economic Development.
Should an IRB Approval or IACUC Approval not be available at the time other hard copy JIT documentation was provided to the NIH or other granting agency, the approval(s) should NOT be forwarded to the agency prior to obtaining the approval of an authorized University official in the OSR or the SPO.
Note: this reflects a deviation from the NIH JIT instructions which permit for the approval(s) to be provided up to two weeks following the submission of other JIT information previously provided with University approval.
Please provide OSR/SPO a copy of the notification from the agency requesting the JIT info.
**University Policy requires that all personnel named in a proposal using human subjects complete the Human Subjects Education Training. Please print and include the Training Certification Letter.
Link to Human Subjects Protection Required Education
OSR Contacts by Sponsor Type (PDF): Listing of the Contract Specialists and the agencies that fall under their authority.