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The Regulatory Support and Advocacy Core provides centralized, accessible regulatory support, advice and guidance.

The OVCR Quality Improvement Program hosts a toolbox of standard tracking forms that helps investigators capture essential information in an organized fashion.

The CCTS Research Navigator helps UIC clinical and translational research investigators and study coordinators find the information and resources needed to navigate research ideas through the university system. The Research Navigator will guide you through a complex research landscape to place you on the right path to the right resources at the right time.

ResearchMatch has a simple goal – to bring together two groups of people who are looking for one another: (1) people who are trying to find research studies, and (2) researchers who are looking for people to participate in their studies.

Bioethics Resources on the Web provides a compilation of web links to information of potential use and interest to diverse audiences—biomedical and behavioral researchers, health care professionals, research participants, patients and patient advocates, students and faculty in different disciplines, and the general public.

Clinical Research Boot Camp is an intensive 3-day training program tailored to meet the specific needs of clinical research personnel and teach them to carry out successful clinical research studies.

ORS assists faculty and staff in proposal development, review and endorsement of proposals, submission of electronic proposals, negotiation and execution of contracts, reporting, receipt and processing of the Notice of Awards (NOA), interpretation of sponsor guidelines, and ensuring compliance with both agency and University policies.

Community Engaged Research Boot Camp an intensive, 3-day program that provides the knowledge and tools research staff need to carry out successful community engaged research projects.

The Centers for Disease Control and Prevention provide information on human participant protection in clinical investigations involving human subjects and the use of drugs, biologics or devices.

The Office for the Protection of Research Subjects (OPRS) provides administrative support for the review and approval of research protocols (experiments) involving humans and human embryonic stem cells (hES).

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