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Research Proposal Template

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RESEARCH PROPOSAL

WHEREAS - RECITALS

WHEREAS, Sponsor Name: (hereafter "Sponsor") desires to fund certain research activities described in this Proposal; and

WHEREAS, Researcher Name / Institution: (hereafter "Researcher") has the expertise and facilities to undertake the proposed research; and

WHEREAS, the parties wish to set forth the scope, deliverables, payment, confidentiality and other terms governing the execution of the research project set forth below.

PROJECT IDENTIFICATION

Start Date:

End Date:

PROJECT SUMMARY

BACKGROUND AND RATIONALE

OBJECTIVES

SCOPE OF WORK AND METHODOLOGY

PAYMENT TERMS

Total Project Funding Amount:

Late Payment:
Payments shall be made against written invoices and are subject to reasonable documentation of work performed. Sponsor may withhold payments for material noncompliance until remedied. Taxes, duties and statutory withholdings are the responsibility of the party as required by law.

TERM AND TERMINATION

Term Commencement Date:    Termination Date:

Either party may terminate this Agreement for convenience upon written notice to the other party delivered at least days prior to the effective date of termination. For material breach, the non-breaching party may terminate if the breach is not cured within days following written notice. Upon termination, Sponsor shall pay for all work performed and non-cancellable obligations incurred through the effective date of termination subject to offset for costs to remedy material defects.

CONFIDENTIALITY

Each party shall maintain in confidence all Confidential Information of the other party disclosed in connection with this Agreement. "Confidential Information" means non-public information designated as confidential or that reasonably should be understood to be confidential given the nature of the information and the circumstances of disclosure. Confidential Information does not include information that: (a) is or becomes generally available to the public other than as a result of a breach of this clause; (b) was lawfully known to the receiving party prior to disclosure; or (c) is independently developed without use of the disclosing party's Confidential Information.

The obligations under this Confidentiality clause shall survive termination of this Agreement for a period of years, except that trade secrets shall remain protected for so long as they meet the legal definition of trade secret.

INTELLECTUAL PROPERTY AND PUBLICATION

Unless otherwise agreed in writing, intellectual property rights arising solely from pre-existing materials remain with their owner. Intellectual property generated solely by Researcher in the performance of this Project shall be owned by . Publication of results shall not be unreasonably withheld; the Sponsor may request confidential review of proposed publications for a period not to exceed days to protect patentable subject matter or confidential information.

COMPLIANCE WITH LAWS AND ETHICS

Researcher shall perform all work in compliance with applicable laws, regulations, institutional policies and accepted ethical standards, including any required human subjects, animal use or biosafety approvals. Researcher shall provide copies of approvals upon Sponsor request.

GOVERNING LAW

This Agreement shall be governed by and construed in accordance with the laws of the jurisdiction of: without regard to conflicts of law principles. Venue for disputes arising under this Agreement shall lie in the courts of that jurisdiction.

ENTIRE AGREEMENT

This document, together with any attachments or exhibits specifically referenced and signed by the parties, constitutes the entire agreement between the parties regarding the subject matter hereof and supersedes all prior and contemporaneous agreements, proposals, and communications, whether oral or written. Any amendment must be in writing and signed by authorized representatives of both parties.

MISCELLANEOUS PROVISIONS

Assignment: Neither party may assign its rights or delegate its obligations under this Agreement without the prior written consent of the other party, except to an affiliate or in connection with a merger or sale of substantially all assets. Independent Contractors: The parties are independent contractors and nothing in this Agreement creates an employment, partnership or joint venture relationship.

Sponsor Name:

By:

Date:

Researcher / Institution:

By:

Date:

Enter text✕

What the Research Proposal Template Is and When to Use It

A Research Proposal Template is a structured document that organizes a project's title, objectives, background, methods, budget, timeline, and required approvals into a single, consistent format. It helps investigators present study rationale and design to sponsors, institutional review boards (IRBs), and collaborators, and provides standard fields for administrative review, compliance checks, and budgetary approval across institutions.

Why a Standard Template Improves Proposal Clarity and Compliance

Using a standardized Research Proposal Template reduces omission risk, ensures consistent presentation to funders and IRBs, and supports institutional review workflows. It clarifies responsibilities, document versions, and submission requirements to help reviewers evaluate scientific merit and budget realism.

Why a Standard Template Improves Proposal Clarity and Compliance

Who Commonly Prepares and Reviews Research Proposals

Principal investigators, research administrators, and grants managers usually prepare the template and coordinate internal approvals before external submission.

  • Principal investigators and co-investigators who shape scope and methods and sign assurance statements.
  • Grants or sponsored research offices that validate budgets, institutional approvals, and compliance items.
  • IRB staff and compliance officers who review human subjects, data privacy, and biosafety elements.

Collaborators, departmental approvers, IRB administrators, and sponsor program officers commonly review and accept the completed proposal document.

Essential Sections Every Professional Research Proposal Contains

A complete Research Proposal Template groups related content into discrete sections — title and administrative data, scientific background and aims, detailed methodology, budget and justification, timeline and milestones, plus references and appendices for supporting materials.

Title and IDs

Project title, funding opportunity number, sponsor name, institutional unit, and a short lay summary so reviewers can immediately identify the submission.

Abstract

A concise summary (typically 250–300 words) that states goals, significance, approach, and expected outcomes for quick reviewer assessment.

Background

Context, prior work, and literature gaps demonstrating why the research matters and how it advances the field.

Objectives & Hypotheses

Clear, measurable aims or hypotheses with primary and secondary endpoints and criteria for success or evaluation.

Methods

Study design, sample size and power, data collection, analysis plan, and risk mitigation steps, described with enough detail for reproducibility.

Budget & Timeline

Itemized costs, personnel effort, indirect cost assumptions, and a milestone schedule showing start, key deliverables, and completion dates.

Fields That Must Be Included in Every Research Proposal

Project Title: Exact project name
Principal Investigator: Full legal name
Institution: Organizational affiliation
Funding Opportunity: Sponsor program identifier
Budget Total: Total direct and indirect costs
Effective Dates: Start and end dates

Step-by-Step: Completing the Research Proposal Template

Follow a consistent sequence: fill administrative fields, draft scientific sections, attach required documents, route for internal approvals, and submit to the sponsor before the deadline.

  • 01
    Start with IDs: Enter title, PI, institution, and sponsor details.
  • 02
    Draft core text: Write abstract, background, aims, and methods.
  • 03
    Prepare budget: Itemize costs, justify expenses, and confirm indirect rates.
  • 04
    Obtain approvals: Route to departmental and compliance reviewers, then submit.

How to Customize the Template for Online Submission

Configure online templates to collect required fields, enforce validation, and automate routing so each submission meets institutional and sponsor-specific rules.

Field Configuration
Required Fields Mark PI, budget, and dates as mandatory.
Conditional Sections Show IRB questions when human subjects flagged.
Authentication Require institutional login or two-factor where needed.
Routing Rules Auto-send to grants office after PI approval.

Where to Send the Completed Research Proposal

Submission paths vary: internal review systems, sponsor portals, and institutional repositories are common. Confirm the sponsor's required method before finalizing the file format.

  • Internal Grants Office: Primary review and institutional signature collection.
  • IRB Submission: If human subjects involved, submit protocol for ethics review.
  • Sponsor Portal: Upload final package before the sponsor deadline.
  • Institutional Repository: Store accepted proposals or data management plans.

Sharing and eSubmission Options for Research Proposals

Choose a delivery method that matches sponsor and institutional requirements: secured upload, email with encrypted attachment, or direct sponsor portal entry.

  • File Formats: PDF, DOCX acceptable
  • Access Controls: Use password or institutional SSO
  • eSignature Methods: Email link, SMS code, or PKI

Typical Timelines and Deadlines to Track

Plan backward from sponsor deadlines and allow time for internal approvals, budget negotiation, and compliance reviews to avoid late submissions.

Sponsor Submission Deadline:

Firm date set by funder; set internal buffer.

Internal Office Review:

Allow at least 7–14 business days for grants office checks.

IRB Review Window:

Initial review can take 4–8 weeks depending on board workload.

Budget Finalization:

Complete at least 5 business days before internal deadline.

Final PI Approval:

Sign and date immediately before upload.

Common Mistakes to Avoid When Preparing a Proposal

  • Incomplete budget detail that omits indirect costs or fringe benefits, leading to institutional pushback and resubmission delays.
  • Missing compliance sections such as human subjects, data management, or biosafety statements, which can halt IRB or institutional review.
  • Using inconsistent names or titles for the PI and institutional signatories, causing identity mismatches during sponsor verification.
  • Late routing for internal approvals that leaves insufficient time to correct reviewer comments before the sponsor deadline.

Consequences of Errors or Late Submissions

Missed Deadline: Sponsor may reject
Noncompliant Budget: Funds withheld or reduced
Incomplete IRB Info: Approval delayed
Name Mismatch: Signature invalidation risk
Unauthorized Signatures: Institution may refuse acceptance
Data Security Lapses: Regulatory exposure

Downloading, Saving and Supporting Documents to Attach

Finalize the proposal in a stable, non-editable format for submission; include required attachments such as CVs, letters of support, facilities descriptions, and data management plans.

Download Formats

Export the final package as PDF/A for archival stability; keep an editable DOCX master for internal revisions.

Required Attachments

Include PI CVs, budget justification, facilities and equipment statements, and letters of collaboration as individual files per sponsor rules.

Version Control

Preserve a dated version history and label files with version and date to prevent accidental overwrites.

Secure Storage

Store signed proposals in an access-controlled repository to meet institutional recordkeeping and auditability needs.

Representative eSignature Pricing and Compliance Comparison

Common eSignature solutions vary by price model, HIPAA support, and bulk-send capabilities. The table below lists representative starting prices and a few feature comparators for vendor evaluation; signNow is listed first per platform comparison conventions.

signNow DocuSign Adobe Sign PandaDoc HelloSign
Starting Price $8/user/mo $15/user/mo $14/user/mo $19/user/mo $15/user/mo
Free Trial 7-day free trial Varies by vendor Varies by vendor Varies by vendor Varies by vendor
Bulk Send Yes Yes Yes Yes No
Audit Trail Yes Yes Yes Yes Yes
HIPAA Compliant Yes Yes Yes No No
Envelope Cap No cap 100 envelopes/user/year Varies by plan Varies by plan Varies by plan

Frequently Asked Questions About the Research Proposal Template

Answers to common questions about e-signatures, notarization, submission format, and recordkeeping for research proposals.


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