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Investigator-Initiated Clinical Trial Planning and Implementation Grants

 

Lock icon: This link will not work for public visitors.Some links will work for NIAID staff only.

Standard Operating Procedure Table of Contents

Purpose

To provide investigators with funds to prepare a) materials NIAID needs to determine a project's feasibility and b) documentation required for applying for the second step, an NIAID Clinical Trial Implementation Cooperative Agreement (U01).

Procedure

Applicants -- R34 Process

  • Read the Clinical Trial Planning (R34) Grants Guide notice for details. Also read Requesting Permission to Submit a Clinical Trial Planning (R34) or Implementation (U01) Grant Application.
  • Speak with the appropriate NIAID division point of contact identified in the Guide notice. That person can answer your questions and refer you to the appropriate program officer.
  • Request approval to submit an R34 application from the program officer.
    • Review the list of information you will need to provide the program officer at Requesting Permission to Submit a Clinical Trial Planning (R34) or Implementation (U01) Grant Application. Before you prepare anything, call the program officer for help with the process.
    • Send NIAID your written request for preapproval at least ten weeks before the receipt date.
    • The program officer sends your request through an internal NIAID approval process.
    • Within six weeks, you will receive a letter signed by the relevant division director or designee informing you whether your request has been approved.
  • If NIAID approves your request, prepare your application using the electronic application package.
  • NIAID special emphasis panel members will peer review your application. Contact the scientific review officer for questions during review, and contact the program officer after review.

Applicants -- U01 Process

  • NIAID R34 recipients may apply for a U01. Read the Clinical Trial Implementation (U01) Cooperative Agreement Guide notice for details.
  • Speak with the appropriate NIAID division point of contact identified in the Guide notice. That person can answer your questions and refer you to the appropriate program officer.
  • For grant applications with budgets that exceed $500,000 in direct costs in any year of the grant, request preapproval to submit a U01 application from the NIAID program officer.
    • Review the list of information you will need to provide the program officer at Requesting Permission to Submit a Clinical Trial Planning (R34) or Implementation (U01) Grant Application. Before you prepare anything, call the program officer for help with the process.
    • Send NIAID your written request for preapproval at least ten weeks before the receipt date.
    • The program officer sends your request through an internal NIAID approval process. For more information about this process, see the U01 Preapproval Process -- Applications With Budgets Over $500,000 in the Program Division Staff and Management section below.
    • Within six weeks, you will receive a letter signed by the relevant division director or designee informing you whether your request has been approved.
    • If NIAID approves your request, you may apply.
  • Prepare your application using the PHS 398 Grant Application. Follow the Clinical Trial Implementation (U01) Cooperative Agreement Guide notice for additional instructions.
  • Send your application in time for CSR to receive it on or before the Standard NIH Receipt Date.
  • NIAID special emphasis panel members will peer review your application. Contact the scientific review officer for questions during review and contact the program officer after review.
  • If successful, you will receive an award about four months after NIH receives your application.
  • If you're unable to complete a trial within the performance period of your award, read the NIAID Policy for Extension of Investigator-Initiated Clinical Trials Guide notice. Contact the program officer listed in this notice to see if NIAID will consider extending your award.

Program Division Staff and Management

Divisions preapprove submission requests based on Institute priorities and available resources.

R34 Preapproval Process

  • The program officer completes Sections A, B, E, and F of the Lock icon: This link will not work for public visitors.Request Form to Accept a Clinical Trial Planning (R34) or Implementation (U01) Grant Application and emails it to the division director.
  • The division director completes Section C of the form. He or she has authority to accept R34 grant applications.
  • After the approval is complete, a program staff member prepares a letter for the division director's signature.
  • The program officer sends the applicant the signed letter stating whether the project was approved.

U01 Preapproval Process -- Applications With Budgets Over $500,000

For an application with a budget over $500,000 in direct costs in any one year, the applicant requests preapproval to submit a U01 application from the NIAID program officer.

  • The program officer completes Sections A, B, E, and F of the Lock icon: This link will not work for public visitors.Request Form to Accept a Clinical Trial Planning (R34) or Implementation (U01) Grant Application and emails it to the division director.
  • The division director has the authority to accept or reject any request with a budget up to $1 million in direct costs for any year, including requests for U01s that follow R34s that had been approved by a division director, peer review, and Council. The division director can also accept or reject a clinical trial that costs between $500,000 and $1 million in direct costs for any year after notifying the Budget and Financial Management Branch.
  • If the request is for more than $1 million in direct costs for any year, the application also goes to the division director's meeting for approval.
  • After this preapproval process is complete, program staff prepare a letter for the division director's signature.
  • The program officer sends the applicant the signed letter stating whether the project was approved. The program officer also submits a copy of the letter to the division director, the DEA contact (see below), and the appropriate division coordinator (see below).

Contacts

Patricia Haggerty, Ph.D.
Division of Extramural Activities
301-451-2615
Email: haggertp@nih.gov

Martin Gutierrez
Division of AIDS
301-451-2703
Email: mgutierrez@niaid.nih.gov

Josiah Wedgwood, M.D., Ph.D.
Division of Allergy, Immunology, and Transplantation
301-496-7104
Email: jwedgwood@niaid.nih.gov

Shy Shorer, M.D.
Division of Microbiology and Infectious Diseases
301-451-3025
Email: shorers@niaid.nih.gov

If you have knowledge to share or want more information on this topic, email deaweb@niaid.nih.gov with the title of this page or its URL and your question or comment. Thanks for helping us clarify and expand our knowledge base.

Links

Lock icon: This link will not work for public visitors.Request Form to Accept a Clinical Trial Planning (R34) or Implementation (U01) Grant

Human Subjects Research Requirements SOP and other Human Subjects SOPs

Investigator-Initiated Clinical Trials Resources main page

Trans NIAID Clinical Research Toolkit

Program announcements

 

Look It Up

See the Glossary for terms.