Joe Larson
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Articles
Recent activity by Joe Larson-
Office of Clinical Research
The Office of Clinical Research (OCR) provides tools and services to help University of Rochester Medical Center faculty and staff with the administration of clinical trials. By streamlining the...
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Grant Writing Resources
Grant Application Materials Need a letter of support from the UR CTSI or boilerplate language for your grants? The UR CTSI can help you with that. See below for steps to request these materials, an...
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NIH Funding Acknowledgement
Cite the CTSA Grant with NIH Funding Acknowledgment The University of Rochester Clinical & Translational Science Institute (UR CTSI) is supported in part by grants UL1 TR002001, KL2 TR001999, and T...
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Population Health Postdoc
Population Health Research Postdoctoral Fellowship This fellowship aims to produce interdisciplinary researchers trained in team science and competency-based skills who can conceptualize researc...
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SCORE
SCORE: Study Coordinators Organization for Research & Education SCORE provides support and regular networking opportunities to University research coordinators and staff. The participants of this U...
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NIH Funding Acknowledgement
Cite the CTSA Grant with NIH Funding Acknowledgment The University of Rochester Clinical & Translational Science Institute (UR CTSI) is supported in part by grants UL1 TR002001, KL2 TR001999, and T...
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Recruitment and Retention
Recruitment Tools Advertising Your Studies Have a question?Contact the URMC Marketing Department. There are many ways to advertise your clinical research studies to recruit participants, including...
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ClinicalTrials.gov Guidance for Required Reporting
Support for ClinicalTrials.gov Study Registration The Office of Regulatory Support (ORS) offers services to support research teams with registration and reporting of clinical research trials at C...
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Regulatory Science - Research and Education
The U.S. Food and Drug Administration (FDA) defines Regulatory Science as “the science of developing new tools, standards, and approaches to assess the safety, efficacy, quality, and performance of...
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Preclinical Studies Guidance for FDA GLP
Good Laboratory Practice (GLP) [21 CFR Part 58] Good Laboratory Practice (GLP) deals with the organization, process and conditions under which laboratory studies are planned, performed, monitored, ...