Clinical Research Coordinator II

Role Overview

• Manages research project databases, develops flow sheets and other study-related documents
• Completes source documents/case report forms
• Provides guidance to less experienced staff
• 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
• Supervises collection of study specimens and processing
• Establishes case packages for study procedures
• Monitors scheduling of procedures and charges
• Ensures compliance with research protocols
• Prepares regulatory submissions
• May perform phlebotomy or diagnostics with appropriate credentialing and training.
• Performs related approved responsibilities as required.

Requirements

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

Benefits

• Emory is an equal opportunity employer
• Equal access and reasonable accommodations for individuals with disabilities upon request