Clinical Research Coordinator managing administrative activities for clinical trials at Emory University. Involved in data management, patient recruitment, and ensuring regulatory compliance in clinical research.
Responsibilities
Maintains data pertaining to research projects
Completes source documents/case report forms
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
Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges
Assists with quality assurance and tracks regulatory submissions
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 licensed practical nursing experience
Bachelor's degree, 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
Clinical training requirements tracked through Emory Healthcare
Remote work from home day options may be granted at department discretion
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