Manages research project databases, develops flow sheets and other study related documents
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
Supervises collection of study specimens and processing
Establishes case packages for study procedures, monitors scheduling of procedures and charges
Ensures compliance with research protocols, reviews case report forms and audits for accuracy
Prepares regulatory submissions
With appropriate credentialing and training may perform phlebotomy or diagnostics.

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
Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred

Emory is an equal opportunity employer
Health and safety information provided
Commitment to ensuring equal access and reasonable accommodations to qualified individuals with disabilities

Clinical Research Coordinator III

About this role