Clinical Research Coordinator II at University of South Florida responsible for coordinating clinical research activities and ensuring participant data quality. Serving as main contact for sponsors and patients for specific research protocols.
About the role
- 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
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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