Clinical Research Coordinator managing the conduct of clinical trials at Emory University. Handling administrative activities and overseeing research project requirements and compliance.
About the role
- Clinical Research Coordinator managing clinical trials at Emory University. Overseeing research projects, providing guidance, and ensuring compliance with protocols and regulations.
Responsibilities
- Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects
- Trains and provides guidance to less experienced staff
- Oversees data management for research projects
- Interfaces with research participants and resolves issues related to study protocols
- Authorizes purchases for supplies and equipment maintenance
- Determines effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials
- Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes
- Monitors IRB submissions and responds to requests and questions
- Interfaces with study sponsors, monitors and reports SAEs; resolves study queries
- Provides leadership in determining, recommending, and implementing improvements to policies/processes
- Assists in developing grant proposals and protocols
- With appropriate credentialing and training may perform phlebotomy, specimens collection or diagnostics
- May perform some supervisory duties
- Performs related approved responsibilities as required
Requirements
- High School Diploma or GED and seven years of clinical research experience
- Or two years of college in a scientific, health related or business administration program and five years of clinical research experience
- Or licensed as a Practical Nurse (LPN) and four years of clinical research experience
- Or bachelor's degree in a scientific, health related or business administration program and three years clinical research experience
- Or master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience
- Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred
Benefits
- Opportunity to work from home regularly
- Flexible weekly schedule based upon business needs
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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