Research Facilitators
Research facilitators work with investigators, coordinators, and other staff to reduce barriers to the research process.
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CTSI: Moving research forward together
The Clinical and Translational Science Institute (CTSI) at the University of Pittsburgh accelerates medical innovation through scientific research and clinical discovery.
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Pitt+Me®
With more than 250,000 participants, Pitt+Me helps speed up medical breakthroughs by connecting researchers and participants with relevant research studies.
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The University of Pittsburgh Clinical and Translational Science Institute (CTSI) is an integral part of the National Institutes of Health (NIH) nationwide network that provides the support necessary to bridge the gap between innovative approaches to research and effective clinical and public health practice and policy.
EXPLORE RESEARCH SERVICES
About Us
We help synthesize University-wide programs and new initiatives to promote a more comprehensive understanding of the tangible benefits to health practice that can be realized from clinical and translational research. We are innovation leaders who take great pride in the number of successful projects with which we have assisted.
WHAT WE DO
Guides & Tools
A collection of research-focused guides and tools to help with all aspects of the research process.
EXPLORE GUIDES & TOOLS
Funding
The latest information about funding announcements, opportunities, support and resources.
LEARN ABOUT FUNDING
Education & Training
Find out about ICRE degree programs, awards, fellowships, and scholarships, in addition to information about seminars and workshops.
EDUCATION & TRAINING INFOMeet Our Team
Our research facilitators and Core divisions offer a wide array of services and specialist knowledge. Together, they can help your research project reach its full potential.
I Need Help
Get in contact with CTSI to learn more about research services, guides and tools, funding opportunities, and more.
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Upcoming Events
Insights:
Participant Recruitment and Engagement
Pitt+Me Registry, a database of more than 200,000 adult and pediatric participants, is an innovative voluntary database of individuals who have consented to be contacted for potential participation in research studies. The registry’s novel software matches participants with studies for which they may be eligible.