Clinical Research Coordinator

Duties And Responsibilities

• Primary Coordinates and implements approved research studies according to the study protocol and the policies of Urology of Virginia Research
• Documents and maintains data for all study related procedures, processes, and events
• Participates in study related meetings (out of state travel), quality control, monitoring visits and audits
• Performs selected administrative duties delegated by Director of Research or principal investigators

Requirements

• Able to read, analyze, and interpret information from technical and scientific protocols and government regulations
• Possess excellent verbal and written communication skills as well as excellent interpersonal skills
• Able to effectively present information and respond to questions from physicians, staff, and patients
• Graduate of either an accredited Medical Assistant / Medical Technologist program, accredited school of professional nursing or possess a Bachelor’s Degree
• Minimum of 2 years’ experience in clinical research or in a clinical office setting (urology preferred)
• Certification by ACRP or SOCRA may be considered in place of education requirements

Equal Employment Opportunity

Equal employment opportunity for all is a very important philosophy for our practice. We will evaluate all applicants and employees without regard to race, color, religion, national origin, sex, age, non-disqualifying disability, history of military service, genetic information, or any other status protected by law.