Jesse Tarbutton B.S., CCRC

Certified Clinical Research Coordinator with more than 15 years research experience. Participates in patient recruitment ensuring proper informed consent, eligibility requirements are met and enrolls patient onto clinical trials Manage patients on research studies ensuring all study required visits are completed per protocol Maintains compliance with protocol requirements and all applicable regulatory requirements Performs accurate and complete data entry, case report form completion and query management Ensure data is enter into clinical trial monitoring systems Appropriately utilizes the electronic medical record for management of the patient on study and to communicate with clinical staff Participate in monitoring visits, site initiation visits and close-out visits as needed