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The Research and Clinical Trials Administration (RCTA) facilitates the timely execution and completion of high-quality research at Rush. The office provides a menu of services to assist Rush investigators and industry sponsors with all aspects of research. The staff has extensive training to ensure that studies are conducted in accordance with sponsors' standards, as well as with federal regulations and current guidelines for good clinical practice. Click the "More" link for more information about Research and Clinical Trials Administration.
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The files listed below are available for download in Word Format using the links below.
- CMS Overview
- Research Billing Plan
- Principal Investigator Entrance Checklist
- Principal Investigator Exit Checklist
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Click on the "More" link to see the full list of services for investigators and sponsors. The first two services for investigators appear below.
Budget development and negotiation of clinical trial agreements
The Research and Clinical Trials Administration Office assists investigators in developing budgets and facilitates negotiations with sponsors.
Study initiation, patient recruitment and follow-up
The office helps investigators and sponsors with all aspects of study start-up, enrollment and retention. Our staff is available to review recruitment opportunities for specific studies.
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NIH Update Form 398 Vertebrate Animal Section (VAS) Requirement