Clinical Research Coordinator II – Infectious Diseases

Role Overview

• Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms
• Provides guidance to less experienced staff
• Interfaces with research participants, determines eligibility and consents study participants according to protocol
• Approves orders for supplies and equipment maintenance
• Assists in developing recruitment strategies and conducting screenings for study participants including interviews and questionnaires
• Supervises collection of study specimens and processing
• Establishes case packages for study procedures, monitors scheduling of procedures and charges, coordinates other services as needed
• Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors
• Prepares regulatory submissions
• With appropriate credentialing and training may perform phlebotomy or diagnostics
• Performs related approved responsibilities as required

Requirements

• High School Diploma or GED and five years of clinical research experience
• Or two years of college in a scientific, health related, or business administration program and three years clinical research experience
• Or a licensed practical nurse (LPN) and two years clinical research experience
• Or a Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience
• Or a Master's degree, MD or PhD in a scientific, health related or business administration program

Benefits

• Emory is an equal opportunity employer
• Reasonable accommodations to qualified individuals with disabilities upon request