Skip to Content

ORA Staff Directory

Directions & Map

Hours & Address

Calendars & Deadlines

Frequently Asked Questions Ethical Guidelines, Federal Regulations and State Statutes HRPP Policies and Procedures Tracking Protocol Status Full Committee Mtg Results Verification of Tutorial Completion

Animal Activities Requiring Review IACUC Policies and Guidelines Application Instructions Application Preparation Checklist Modifications to Approved Protocols Closing a Protocol

Proposal Preparation Sponsor ERA Systems Intro to Grants.gov eLearning Course Preparing a Grants.gov Submission Pre-Award Administration Post-Award Administration e-Synopsis Closeout Contract and Grant Reports

About the COI Oversight Committee Reasons to Disclose Areas of Risk Disclosure Requirements Chart

The Starting Point Confidential Disclosure Agreements (CDA) Negotiation and Execution of Clinical Trial Agreements Clinical Trial Master Agreements Frequently Asked Questions

FAQ Export Control Regulations .ppt Deemed Export Tool .ppt Travel to Embargoed Countries

What is Stem Cell Research? Fiscal Guidance to Investigators and Administrators Stem Cell Review Procedures Resources

Electronic Research Tutorials Responsible Conduct of Research HRPP In-service Training Request Form SPA In-service Training Request Form RAMP

The Starting Point

When participation in a Clinical Trial appears likely, notify and submit to Sponsored Projects a complete Proposal Packet consisting of the following documents:

Original Administrative Approval Form
- Sponsor contact name, phone number, and e-mail address
Request for Exception to Principal Investigator Eligibility, if required.
700-U Financial Disclosure Form for Principal Investigator and/or Co-Principal Investigator
- 700-U Addendum (If positive 700-U)
Clinical Trial Principal Investigator Questionnaire
Draft Budget
Copy of Protocol
Draft Agreement