Data Coordinator II supporting clinical trials research at Winship Cancer Institute. Facilitating data management and ensuring accuracy of clinical trial databases with compliance to protocol guidelines.
About the role
- Clinical Research Coordinator managing aspects of clinical trials at Winship Cancer Institute. Handling data management, participant interface, and overseeing trial compliance in Atlanta.
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
Requirements
- High School Diploma or GED with seven years of clinical research experience
- Two years of college in a scientific, health related or business administration program and five years of clinical research experience
- Licensed as a Practical Nurse (LPN) with four years of clinical research experience
- Bachelor's degree in a scientific, health related or business administration program with three years clinical research experience
- Master's degree, MD or PhD in a scientific, health related or business administration program with one year of clinical research experience
- Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred
Benefits
- Health and Safety Information
- Equal opportunity employer
- Reasonable accommodations for qualified individuals with disabilities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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