Clinical Research Coordinator I – Radiology and Imaging Sciences

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
• Performs related approved responsibilities as required.

Requirements

• High School Diploma or GED and three years of administrative support experience
• Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience
• Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience
• Or a Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.
• All clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.

Benefits

• Health and Safety Information
• Equal opportunity employer