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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
Primary Contact

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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