¶¶Òõ¶ÌÊÓÆµ

Research Grant Agreement Template for United States

Create a bespoke document in minutes,  or upload and review your own.

4.6 / 5
4.8 / 5

Let's create your Research Grant Agreement

Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Get your first 2 documents free

Your data doesn't train Genie's AI

You keep IP ownership of your information

Key Requirements PROMPT example:

Research Grant Agreement

"I need a Research Grant Agreement for a three-year medical research project funded by a private foundation, with specific provisions for handling patient data and potential commercialization of research outcomes, starting March 2025."

Document background
Research Grant Agreements are essential documents in the U.S. research ecosystem, used whenever financial support is provided for scientific, medical, or academic research projects. These agreements define the parameters of the funding relationship, ensuring compliance with federal and state regulations while protecting the interests of all parties involved. A Research Grant Agreement typically includes detailed provisions for project scope, funding disbursement, compliance requirements, intellectual property rights, and reporting obligations. It's particularly crucial for maintaining transparency and accountability in research funding, whether from government agencies, private foundations, or other funding sources.
Suggested Sections

1. Parties: Identifies the grantor (funding entity) and grantee (recipient institution/researcher)

2. Background: Outlines the purpose of the grant and research context

3. Definitions: Key terms used throughout the agreement

4. Grant Award: Details of funding amount, payment schedule, and disbursement conditions

5. Project Scope: Detailed description of the research project, objectives, and deliverables

6. Duration: Project timeline, start date, end date, and any extension provisions

7. Reporting Requirements: Financial and technical reporting obligations

8. Intellectual Property Rights: Ownership and rights to research outcomes and innovations

9. Termination: Conditions for early termination and consequences

Optional Sections

1. Human Subjects Protection: Required provisions and compliance requirements when research involves human participants

2. Animal Research Provisions: Compliance requirements and protocols for research involving animal subjects

3. Export Control: Provisions for compliance with international research restrictions and sensitive technology handling

4. Data Management: Requirements for data handling, storage, sharing, and protection

Suggested Schedules

1. Schedule A - Project Description: Detailed research proposal and methodology

2. Schedule B - Budget Breakdown: Detailed financial allocation and allowable costs

3. Schedule C - Timeline and Milestones: Detailed project schedule and key deliverables

4. Schedule D - Reporting Templates: Standard forms for progress and financial reporting

5. Schedule E - Key Personnel: List of principal investigators and key research staff

6. Schedule F - Compliance Certificates: Required regulatory approvals and certifications

7. Schedule G - Equipment Schedule: List of major equipment to be purchased or used in the research

Authors

Alex Denne

Head of Growth (Open Source Law) @ ¶¶Òõ¶ÌÊÓÆµ | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

Clauses

































Industries

Federal Grant Regulations: Primary federal regulations including Uniform Administrative Requirements (2 CFR 200), Federal Grant and Cooperative Agreement Act, and Federal Funding Accountability and Transparency Act (FFATA)

Research Subject Protection: Common Rule for Human Subject Protection (45 CFR 46), Animal Welfare Act, and NIH Guidelines for Research Involving Recombinant DNA

Intellectual Property Framework: Bayh-Dole Act for federally funded research, Patent Act, Copyright Act, and Trade Secrets Act considerations

Financial Compliance: Single Audit Act, Anti-Kickback Statute, and False Claims Act requirements for financial oversight and compliance

Privacy Regulations: HIPAA for medical research, FERPA for educational institutions, and applicable state-specific data privacy laws

Employment Law Compliance: Fair Labor Standards Act, Equal Employment Opportunity laws, and relevant state-specific employment regulations

Tax Regulations: IRS regulations regarding grant funding and state-specific tax implications for research grants

Institutional Policies: University/Research Institution specific policies, Conflict of Interest guidelines, and Research integrity requirements

Industry-Specific Requirements: FDA, EPA, and other agency-specific regulations depending on research field and scope

State-Level Compliance: State grant regulations, procurement laws, and research-specific requirements varying by jurisdiction

Teams

Employer, Employee, Start Date, Job Title, Department, Location, Probationary Period, Notice Period, Salary, Overtime, Vacation Pay, Statutory Holidays, Benefits, Bonus, Expenses, Working Hours, Rest Breaks,  Leaves of Absence, Confidentiality, Intellectual Property, Non-Solicitation, Non-Competition, Code of Conduct, Termination,  Severance Pay, Governing Law, Entire Agreemen

Find the exact document you need

Tech Transfer Agreement

A U.S.-governed agreement facilitating the transfer of technology and related intellectual property rights between entities.

find out more

Confidentiality Agreement In Research

A U.S.-compliant legal agreement protecting confidential information shared during research activities.

find out more

Focus Group Participation Agreement

A U.S.-compliant agreement governing the terms of participation in focus group research, including confidentiality and compensation terms.

find out more

Clinical Research Contracts

U.S.-governed agreement establishing terms and conditions for clinical research studies between sponsors, institutions, and investigators, ensuring regulatory compliance and human subject protection.

find out more

Interview Consent Agreement

A U.S.-compliant legal agreement securing informed consent for conducting and using interview content, protecting both interviewer and interviewee rights.

find out more

Biobank Agreement

A U.S.-governed agreement establishing terms for biological specimen collection, storage, and research use, compliant with federal and state regulations.

find out more

Clinical Trial Contract

A U.S.-governed agreement that establishes terms and conditions for conducting clinical trials, ensuring regulatory compliance and defining party responsibilities.

find out more

Clinical Research Agreement

A legal agreement governing clinical research activities in the United States, ensuring compliance with FDA and HIPAA regulations.

find out more

Confidential Disclosure Agreement In Clinical Research

A U.S.-compliant agreement protecting confidential information exchanged during clinical research activities.

find out more

Invention Disclosure Agreement

A U.S. legal document used to formally document and protect new inventions while maintaining confidentiality and establishing ownership rights.

find out more

Market Research Agreement

A U.S.-governed contract establishing terms between a market research provider and client, defining research scope, deliverables, and compliance requirements.

find out more

Indirect Cost Agreement

A U.S. federal document establishing approved indirect cost rates and methodologies for organizations receiving federal funding.

find out more

Technology Development Agreement

A U.S.-governed agreement establishing terms for technology development projects, including IP rights, milestones, and payment terms.

find out more

Research Grant Agreement

A U.S.-governed legal agreement establishing terms and conditions for research funding between a grantor and grantee institution.

find out more

Clinical Trial Confidentiality Agreement

A U.S.-compliant agreement protecting confidential information shared during clinical trials, ensuring HIPAA and FDA compliance.

find out more

Biological Material Transfer Agreement

A U.S.-compliant agreement governing the transfer of biological materials between organizations, establishing terms for usage and protecting intellectual property rights.

find out more

Research And Development Agreement

A U.S.-governed agreement establishing terms for collaborative research and development activities between parties.

find out more

Clinical Study Agreement

A U.S.-governed agreement establishing terms and conditions for conducting clinical research, including responsibilities of parties and regulatory compliance requirements.

find out more

Contract Research Agreement

A U.S.-governed agreement establishing terms for contracted research services, including scope, IP rights, and payment terms.

find out more

Collaboration Research Agreement

A U.S.-governed agreement establishing terms for joint research activities between multiple parties, including IP rights and confidentiality provisions.

find out more

Download our whitepaper on the future of AI in Legal

By providing your email address you are consenting to our Privacy Notice.
Thank you for downloading our whitepaper. This should arrive in your inbox shortly. In the meantime, why not jump straight to a section that interests you here: /our-research
Oops! Something went wrong while submitting the form.

³Ò±ð²Ô¾±±ð’s Security Promise

Genie is the safest place to draft. Here’s how we prioritise your privacy and security.

Your documents are private:

We do not train on your data; ³Ò±ð²Ô¾±±ð’s AI improves independently

All data stored on Genie is private to your organisation

Your documents are protected:

Your documents are protected by ultra-secure 256-bit encryption

Our bank-grade security infrastructure undergoes regular external audits

We are ISO27001 certified, so your data is secure

Organizational security

You retain IP ownership of your documents

You have full control over your data and who gets to see it

Innovation in privacy:

Genie partnered with the Computational Privacy Department at Imperial College London

Together, we ran a £1 million research project on privacy and anonymity in legal contracts

Want to know more?

Visit our for more details and real-time security updates.