UAMS Office of Research Regulatory Affairs (ORRA) 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 IND or IDE, we 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 - Cesiley Trevino, MSHP, CCRP, CRS
Clinical Research Monitoring Manager
CTrevino@uams.edu - Crystal Smith, MSW, MA
Clinical Research Monitoring Specialist
CSmithb2a5@uams.edu - Ashley Clark, MPH, CHES
Clinical Research Monitoring Specialist
ABoureimamorou@uams.edu