Covered under University series concept / job specification for classification 4722. Under general direction works on operational and/or procedural assignments that require the exercise of considerable discretion and independent judgment. Understands implications of work and makes recommendations for solutions. Determines methods and procedures on new assignments. Individual will perform the following tasks, but not limited to: assume ACRC duties (pre-screen/screen patients, schedule patient visits and follow-ups, communicate with investigators/ RNs/other departments/sponsors, assist investigators with consenting and research visits, demonstrate thorough interpretation and management of protocols, assist with study logistics, attend departmental meetings) abstract data from the electronic medical records, research chart and other source documentation enter clinical research patient data into electronic databases support the clinical research coordinator(s) and manager as needed enter data into the institutional Clinical Trial Management System, On. Core What It Takes to be Successful Required: Thorough knowledge in administrative procedures and processes including word processing, spreadsheet and database applications. Requires good verbal and written communication skills, active listening, critical thinking, multi-task and time management skills. Requires interpersonal and work leadership skills to provide guidance to other nonexempt personnel. Understanding of Medical Terminology Experience scheduling meetings/conferences Experience calendaring/filing Experience with letter composition Experience with Data Entry (MS Word/ Excel) High school diploma or equivalent experience 1-3 years relevant experience or combination of experience and education Pay Rate: $29.40/hour Total Rewards