Clinical Research Coordinator I

Role Overview

• Handles or assists with the administrative activities generally associated with the conduct of clinical trials
• Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry
• Assists with patient recruitment
• Attends study meetings
• Orders and maintains equipment and supplies
• Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires
• Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping
• Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges
• Assists with quality assurance and tracks regulatory submissions

Requirements

• High School Diploma or GED and three years of administrative support experience
• Two years of college in a scientific, health-related, or business administration program and one year of admin support or customer service experience
• Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience
• Bachelor's degree, Master's degree, MD, or PhD in a scientific, health-related, or business administration program

Benefits

• Equal opportunity employer
• Consideration for employment without regard to race, color, religion, sexuality, national origin, disability, protected veteran status
• Reasonable accommodations to qualified individuals with disabilities upon request