Brittney Harbin

Experience

1. Senior Clinical Research Associate

   ICON plc

   Apr 2024 — Present · Arlington, VA, US

   Identify, select, initiate, and close-out appropriate investigational sites for clinical studies -Monitor those sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs/WPs, applicable regulations and the principles of ICH-GCP-Manage studies and provide staff training and contribute to the review of ICON systems and procedures as appropriate -Provide a benchmark of monitoring competence to inexperienced / less experienced colleagues-Coordinates all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation-Participates in the evaluation of potential clinical sites according to established criteria of acceptability-Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials-Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions-Conduct study termination visits, obtain final reports from investigators, and participate in the preparation of final reports for regulatory submission

Education

• The University of North Carolina at Chapel Hill

  Bachelor's degree

  2009 — 2013

• Louisiana State University Health Sciences Center

  Master of Public Health - MPH

  2016 — 2018