Summary and quick links
SOM Emergency Preparedness and Response Sheets
SOM offices supporting research (includes institutional information for grant proposals)
Help for new faculty
Sponsored research and consulting agreements
Staff and trainees
Research supplies, equipment, travel
Human subjects research
Intellectual property, confidentiality, entrepreneurial activities
Facilities: renovation and repair
Environmental health and safety
Other compliance issues and training
SOM core facilities and collaborators
SOM research facilities: current and planned construction and major renovations
Questions concerning the Office of Grants and Contracts:
How does the Office of Grants and Contracts support research at the SOM?
The office provides: institutional approval of proposals; interpretation of sponsor policies; assistance with budget development; post-award assistance (extensions, changes in work scope, close-out, etc.); with UVA Office of Sponsored Programs, negotiation of clinical trials, research, materials transfer, confidentiality, and consulting agreements. Contact: Stewart Craig, Assistant Dean for Research Administration.
How does SOM Grants and Contracts differ from UVA Sponsored Programs?
Grants and Contracts carries out most of the functions of the Office of Sponsored Programs (OSP) on behalf of SOM faculty. The exceptions are post-award financial management (responsibility of OSP), negotiation of contracts and agreements (both offices), and consulting agreements (responsibility of Grants and Contracts).
How many copies of proposals must be routed to the Office of Grants and Contracts? Two (for G&C and for Sponsored Programs).
How should effort be reported? Professional staff should report effort as a percentage of time; non-professional effort should be reported as hours per week.
Where can I find the institutional information required by sponsors on proposals? See below:
University of Virginia
PO Box 400195
Charlottesville, VA 22904
Official to be notified of award:
Director for Grants & Contracts
Office of Sponsored Programs
University of Virginia
PO Box 400195
Charlottesville, VA 22904
Signing official for the applicant organization:
Stewart P. Craig
Assistant Dean for Research Administration
Director, Office of Grants and Contracts
University of Virginia
PO Box 400195
Charlottesville, VA 22904
PHS entity number: 1546-001-796A1
UVA tax ID number: 546-001-796
Congressional district: fifth (reported on SF424 form as "VA-005")
NSF awardee organization code: 0037457-02
Institutional Profile Number: 1526402
Other institutional information: see the Office of Sponsored Programs site
Questions concerning other SOM offices supporting research:
What are the responsibilities of the Office for Research?
Financial conflict of interest; dissemination of targeted funding opportunities; volunteers in research; management of research space and core facilities; assistance with complex grant and contract proposals; and medical student research opportunities. Contact: Dr. Steven Wasserman, Assistant Dean for Research.
How does the Clinical Trials Office support clinical research?
Mentoring of clinical research coordinators; protocol development and preparation; continuing education; study monitoring; and quality assurance. Contact Lori Elder, Director.
What are the responsibilities of the Graduate Programs Office?
Administrative support for Biomedical Sciences graduate programs and SOM postdoctoral fellows; data collection/management/reporting and other support for training grant proposals and institutional reports; undergraduate Summer Research Internship Program. Contact: Dr. Joel Hockensmith, Assistant Dean for Graduate Research and Training.
Where can I find information on research funding programs?
The Office for Research sends targeted announcements of external funding opportunities to faculty and departments/centers. The Office's web site also provides strategies for finding funding. Additional information...
How do I apply for funding?
Principal Investigators are strongly urged to seek a collegial review before submitting a proposal. Departmental and Office of Grants and Contracts approvals are required prior to submission of any proposal. Your administrator should help you generate budgets and application forms and forward the proposal to the Office of Grants and Contracts for review and approval. Additional information...
Who can help me prepare clinical trials budgets and invoice for trial expenses?
The Clinical Trials Office can help investigators prepare clinical trials budgets, negotiate budgets with sponsors, and invoice sponsors as study milestones are achieved. Additional information...
Can I consult externally as a SOM employee?
UVA policy permits faculty to consult one day in seven (one per calendar week), but the SOM restricts the allowance for its faculty to 45 days per year (total annual leave, consulting, and sick days). The SOM policy on consulting and professional activities requires that all consulting agreements be reviewed by the Office of Grants and Contracts prior to approval.
How do I hire staff?
Contact your department HR administrator to create positions within the UVA HR system, advertise for and interview candidates, and offer positions. Additional information...
What financial and other support are available to graduate students?
In general, the SOM provides the first year of student stipends; thereafter, they are supported financially by training grants, research grants, or departmental funds. Additional information...
What information and support are available to postdoctoral trainees?
Consult the UVA Postdoctoral Office for information on housing, visas, benefits, tax issues, etc.
May visitors or volunteers participate in my research?
Submit a SOM volunteer agreement to the Dean's Office for approval prior to the visitor's arrival. Note: there are restrictions on UVA volunteers holding certain visas. Refer to the volunteer agreement for additional information.
How do foreign employees and trainees obtain and maintain visas?
Your department or center HR administrator should work with the Dean's Office (see list of SOM department contacts for faculty and Professional Research Staff - requires log-in) and the International Studies Office (non-employee scholars) or University HR (non-citizen employees) to apply for and maintain visas.
What training is available for UVA supervisors?
All supervisors must take training on Preventing Sexual Harassment and Preventing Employment Discrimination through the Office of Equal Opportunity Programs and training on supervising UVA personnel (HR site).
How do I order research supplies, equipment, and services?
Orders are placed through the on-line UVA Marketplace. Your administrator can arrange access to that system and can facilitate the purchase of large equipment and services. Many assays and other services, including the use of shared equipment, are available from SOM research core facilities.
How can I arrange and get reimbursed for job-related travel?
See your administrator and access Procurement Services's guidelines and tips on travel. Requires pre-travel approval and post-travel reimbursement.
Where can I find information on clinical research?
The SOM Clinical Trials Office's Orientation Manual is a compendium on the subject of clinical trials (Good Clinical Practice, ethics, protocol submission, managing trials, etc.). Also refer to our site on clinical research.
How can I get help in developing human use protocols and case report forms (CRFs)?
Contact the SOM Clinical Trials Office. The Division of Biostatistics & Epidemiology (Dept. of Public Health Sciences) can help with study design, analytic plans, and analysis of preliminary data to support protocol development.
Does the institution support development, submission, and maintenance of FDA Investigational New Drug Applications (INDs) and Investigational Device Exemptions (IDEs)?
INDs and IDEs are required for clinical trials of new drugs and devices and of approved drugs that are tested beyond the limits of current product licensure. Contact the Clinical Trials Office for help in developing, submitting, and maintaining FDA applications.
How do I submit protocols to the IRB?
First, take on-line IRB training. If you have not yet arrived at UVA, you can log on as a guest. Submission of protocols and requests for IRB exemptions are facilitated via this site.
What training and professional development opportunities are available for my clinical research coordinator (CRC)?
The IRB-HSR requires on-line training for clinical coordinators and offers a voluntary program on IRB and broader issues. The Clinical Trials Office conducts continuing education, informal discussions, clinical research professional meetings, and mentoring of CRCs.
How do I recruit research subjects?
The Health System web site lists current clinical trials ( click here to advertise your trial). See IRB-HSR advertising guidelines for clinical studies. Clinicaltrials.gov is another way to broadcast one's clinical study beyond the University.
Does UVA have a research pharmacy to support clinical research?
The Medical Center's Investigational Drug Service can receive, log, prepare, and blind study drugs. Contact them to discuss services and fees that you should build into your study budget.
Can I access clinical coordinators and clinical space for my investigator-initiated research?
The Clinical Trials Office will provide coordinator support for SOM investigators.
What office supports quality assurance and monitoring activities?
The Clinical Trials Office helps investigators prepare and maintain SOPs and prepare for sponsor/FDA audits, and monitors investigator-initiated studies.
Where/how can I register my own clinical trials on-line?
Sponsors of UVA clinical studies should register at http://prsinfo.clinicaltrials.gov/. Note that the International Committee of Medical Journal Editors requires that registration of Phase 1 clinical trials at a public site before they can be published in those journals.
What resources are available for retrospective research using hospital patient data?
The UVA Clinical Data Repository provides clinical information for the retrospective analysis of health care data.
How can I protect and develop my own intellectual property (IP)?
Submit invention disclosures to the UVA Licensing and Venture Group (formerly the Patent Foundation), who will advise you on patenting and licensing. Additional information...
Who negotiates and signs confidentiality and material transfer agreements?
The Office of Grants and Contracts is responsible for negotiating both "incoming" and "outgoing" agreements. Additional information...
Is there help available to start a company to commercialize my intellectual property?
For an overview of the entrepreneurial process, see the UVA Faculty Entrepreneur's Guidebook. The UVA Patent Foundation can provide help during start-up, including short-term rental of research lab space. The Darden School's Batten Institute can help you develop your business plan and with other aspects of creating and managing a company.
How do I renovate my research space?
You and your research administrator should work with Facilities Management to perform renovations.
How do I request emergency and non-emergency repairs of facilities?
Emergencies: phone Physical Plant (x4-2267) - the line is staffed 24/7.
Non-emergencies: submit a work order to Physical Plant.
What approvals are required in order to use recombinant DNA, toxins, select agents, human tissues, or pathogens?
Contact the Institutional Biosafety Committee to register your proposed research, obtain training, and arrange a lab inspection prior to receiving or using such materials.
What approvals and training are required in order to use hazardous biological, chemical, and radioactive agents?
Contact the Office of Environmental Health and Safety for specific requirements and a schedule of training sessions. Don't forget to obtain training on shipping of infectious substances or diagnostic specimens, if applicable.
What other materials are available for new employees and other personnel participating on my reseach (lab or clinically based)? The SOM has developed an overview of safety issues associated with research areas, which covers training, life safety, where to go in the case of injury or if you have concerns about research safety practices, etc. It is recommended that all new personnel be required to review/provided with a copy of this document before initiating any resaerch activities, as a "best practice."
What other training must I take?
HIPAA privacy training is available via the Health System's NetLearning system. All SOM employees also must complete the UVA Information Technology and Communication (ITC) on-line computer security program.
Who offers training in responsible conduct of research (RCR)?
Trainees on federal training grants are required to take BIMS 710, which is coordinated by the Graduate Programs Office. Individuals may audit the course, but may not participate in small-group sessions. Additional information...
Whom do I contact to discuss financial conflicts of interest (COIs)?
Contact the Office for Research/Dr. Steven Wasserman or the UVA Conflicts of Interest Committee (Dr. Patricia Tereskerz, Chair). Additional information...
Who is responsible for tracking the financial status of my accounts?
Principal Investigators are legally responsible for all expenditures on their accounts and must approve their financial statements every month. Your department administrator should provide reports of expenditures as recorded in the Oracle financial system, for your review and approval. Additional information on roles and responsibilities...
What are my responsibilities concerning effort reporting?
Faculty and research staff must periodically report their effort expended on various activities via the UVA Time and Effort Reporting System. Your administrator can describe any departmental methodology for tracking effort and discuss the content of your effort report prior to your certifying the document. It is important for you to maintain records of your external activities (travel to professional meetings, seminars at other institutions), in case an audit is performed.
Who can assist with computer purchase and set-up and with connectivity issues?
Your department administrator should refer you to your Local Support Partner (LSP), who can discuss equipment specifications and set up new computers purchased on University funds. Depending on the department or center where you reside, your local area network may be supported by UVA Information Technology & Services, Health System Computing Services, or departmental personnel and servers.
How can I obtain UVA discounted or site-licensed software?
Information Technology and Services offers several PC and Mac applications for downloading (note program-specific restrictions on use). Cavalier Computers offers academic discounts on software for personal use.
Whom do I contact in case of property loss or injury?
In case of injury, immediately phone 911 for emergency help. UVA Human Resources handles claims for workers' compensation. Your administrator can help file a claim with Risk Management for reimbursement of property losses.
How do I contact police/security?
Contact HS Security or UVA Police to report a crime or to request a security assessment of your facilities. In an emergency, phone 911. For non-emergent issues:
- Health System Security: 924-5048
- UVA Police: 924-7166
How do I submit an animal protocol?
Access the IACUC's protocol submission system.
How do I order research animals?
You must have an IACUC-approved protocol before you can order animals. Vertebrate animals are ordered by the Center for Comparative Medicine. See their procedures for ordering and deadlines. Animals are delivered 4 to 5 business days after the ordering deadline.
How do I request additional animal cages?
Contact the Center for Comparative Medicine for approval of additional cage space.
What is Occupational Health?
This is a required health program for individuals who work with research animals.
What research core facilities are available at the SOM?
The several institutional core facilities offer access to services and specialized equipment. Additional cores are provided by research centers and complex research awards.
Should I create any policies for my own research group?
You are strongly urged to create policies on authorship and data integrity (including manipulation of graphics) that are tailored to your research program. Creating and adhering to such policies will reduce the potential for authorship disputes and research misconduct. Additional details here.
Where can I find resources to help in managing and maintaining the integrity of my research data?
Read the HHMI publication "Making the Right Moves" on data recording, witnessing, retention, and security. The Office for Research/Dr. Steven Wasserman can provide recommendations tailored to your research program. Additional information on research recordkeeping...
Where can I find the institutional and SOM policies governing research?
Refer to this list of research policies.