Clinical trials are research studies to test the safety or efficacy of a potential medical treatment. This could be drug testing, device testing, diagnostic testing, or procedure testing on humans.
Clinical trials are routed and reviewed in RAMP. They require both a Funding proposal record (FP) required to create the award account, and an agreement record (AGR), required for the agreement to be reviewed by RSP.
- Please route all information on a RAMP record to SMPH, The Org Cost Center Hierarchy (CCH) ID will be CCH000075.
- Attach the agreement (Word version preferred)
- Attach the OnCore ancillary report so that whenever hospital services are being used, the same price is used in all clinical trials.
- Sponsor name and contact information.
- Industry-Sponsored Clinical Trials: The RAMP Funding Proposal record must include a total estimated budget amount. This budget should reflect the anticipated total costs for the clinical trial, including startup costs, total participant enrollment, and other associated expenses, assuming maximum participant enrollment. See the RAMP Job Aid for CTA Budget Entry for additional instructions.
- Federal (direct and flow-through) Clinical Trials: A full budget must be entered in the RAMP Funding Proposal record.
Details and important CTA considerations
To find the industry sponsored clinical trial budget template, please visit the Clinical Trials Institute webpage.