Off-Site Clinical Research Coordinators

This service is provided by the Clinical Research Resource (CRR).

Overview

Irving Institute-funded research coordinators/nurses are available to support pediatric and adult clinical research activities in the Emergency Department, Pediatric Intensive Care Unit (ICU), Neonatal ICU, Neurological ICU, Neurosurgical ICU and Obstetrics and Gynecology department. Traditional research approaches do not allow a flexible framework for these high-risk units to engage in clinical research. Our experienced research coordinators are available to support protocol development, assist with IRB submissions, recruit participants, and collect research data in these clinical areas. The offsite coordinators hold weekly update meetings with the clinical unit manager and monthly meetings with the directors to provide an overview of the regular offsite unit activities. These experienced personnel support clinical research by assisting with:

  • Protocol development
  • IRB submission
  • Participant recruitment
  • Research data collection
  • Regulatory documents

Starting in March 2020, we are also providing support for COVID-19 research. 

Eligibility

All investigators with clinical research studies needing implementation in the offsite-supported units are eligible for this service.

Cost

There is no cost for this service.

Cite it, Submit it, Share it!

If your research has benefited from one or more Irving Institute resources, please remember to:

  • Cite our CTSA grant, UL1 TR001873, in any relevant publications, abstracts, chapters, and/or posters.
  • Submit your publications to PubMed Central (PMC) for compliance with the NIH Public Access Policy.
  • Share your research updates with us by sending an email to: irving_institute@cumc.columbia.edu

Contact

Off-Site Clinical Research Coordinators
622 West 168th Street, 10th Floor
New York, NY 10032
United States