Clinical Research Coordinator I

Role Overview

• Supports and assists in all aspects of clinical data management
• Primary Data Coordinator (DC) for therapeutic and non-therapeutic clinical trials across all disease teams
• Reviews information from medical records to extract data for assigned research protocols
• Accurately captures and enters data into clinical trial databases
• Collects and maintains complete records and metrics on each research study participant
• Consolidates clinical data and reports for investigators as needed
• Attends study team meetings and provides updates regarding protocol data management activities
• Attends protocol related training meetings and completes all required study training
• Prepares for and assists with internal quality control audits

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

• Emory University is an equal opportunity employer
• Offers reasonable accommodations to qualified individuals with disabilities