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Research and Innovation: Office of Research Regulatory Affairs
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  1. University of Arkansas for Medical Sciences
  2. Research and Innovation
  3. Office of Research Regulatory Affairs
  4. Departments
  5. Regulatory Affairs
  6. Monitoring Unit

Monitoring Unit

The Office of Research Regulatory Affairs Monitoring Unit is responsible for monitoring all UAMS-sponsored investigator initiated clinical research trials conducted under an Investigational New Drug application (IND) or Investigational Device Exemption (IDE). If your research study requires an Investigational New Drug application or Investigational Device Exemption, this group will work with you to ensure your study is monitored as required by federal regulations (21 CFR 312.56 and 21 CFR 812.40).

Contact the Office of Research Regulatory Affairs Monitoring Unit at ORRAMonitoringUnit@uams.edu.

Staff Contacts

  • Laura Adkins, MAP, CCRP, CCRA, CRS, AdvCRS
    Director of ORRA
    LLAdkins@uams.edu
    501-686-6092
  • Cesiley Trevino, MSHP, CCRP, CRS
    Clinical Research Monitoring Manager
    CTrevino@uams.edu
    501-526-7384
  • Jennifer Hendrix, BSN, RN
    Clinical Research Monitoring Specialist
    JLHendrix@uams.edu
    501-603-1638

Subpages

  • Study Monitoring
  • Study Management Tools
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Mailing Address: 4301 West Markham Street, Little Rock, AR 72205
Phone: (501) 686-7000
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