Stanford

Proposal Preparation and Submission

Set-Up Your Study

The STUDY SET-UP stage includes activities that occur after the study has been designed and developed, and before you begin to enroll patients.

This stage includes activities in areas such as:

  • contracts & grant proposals
  • IRB approval
  • research management compliance
  • study budgeting & billing
  • required registration of trial
Roles and Responsibilities

Research Management Group describes roles and responsibilities for proposal preparation and submission.

Institutional Facts

Both Research Management Group and DoResearch provide institutional facts such as:

  • Applicant Organization Name and Miscellaneous References
  • Tax Exempt Status
  • Federal Tax Payer ID Number
  • Animal Subjects Approval
  • Boilerplate text for proposals

    Boilerplate text describing programs, resources and facilities – download these Word documents; you can edit as necessary to fit your needs.

    Clinical Trials

    See the RMG website: Clinical Trial Program and Resources for information such as:

  • Clinical Trial Process Flow Chart
  • Clinical Trial Roles and Responsibilities
  • Clinical Educator PI Waiver - Industry Sponsored Clinical Trials
  • Clinical Trial Budget Development Fee
  • Clinical Trial IDC Rate Memo
  • IRB Review Fees
  • Subawards under Clinical Trials

  • QuickLinks