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The mission of the Chicago Biomedical Consortium is to stimulate collaboration among scientists at Northwestern University, the University of Chicago, and the University of Illinois at Chicago that will transform research at the frontiers of biomedicine.
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.
The Atlanta Clinical & Translational Science Institute has kindly shared their Ethical Dilemmas in Scientific Research and Professional Integrity website, video, and podcast with each CTSA.
This web page presents 40+ case scenarios involving responsible conduct in research. Each case is followed by a brief, expert opinion that suggests strategies for resolution. These resources have proven useful as teaching aids and are broadly relevant across the research spectrum. Please help us spread the word!
The UIC Health Science Library's Clinical and Translational Science Research Guide is a compilation of resources available through and recommended by the Health Sciences Library. Included are reporting tools, databases, and author tools.
If you are experiencing computational, data storage or networking bottlenecks on traditional user/lab workstations and/or you are considering using cloud for your research, SABER can be an effective solution both in terms of function and cost.
SABER will operate on a pay-per-use basis, providing researchers with the flexibility to pay for used time/storage and ensures a good return on investment. Researchers can learn more about SABER specs, their competitive rate structure and order process here.
The Library of the Health Sciences offers workshops focused on instruction and consultation in locating and evaluating scientific research indexed in scholarly databases (e.g., Medline, Embase) and in grey (unpublished) literature.
The CCTS collaborated with members of the Office of the OVCR Quality Improvement Program to develop a set of standard case report forms. The forms should be useful for any investigator initiated clinical trials and can be customized to an individual study.