Clinical Research Coordinator managing aspects of clinical trials at Winship Cancer Institute. Handling data management, participant interface, and overseeing trial compliance in Atlanta.
About the role
- Clinical Research Coordinator overseeing multi-site orthopedic clinical studies, providing comprehensive information and ensuring compliance with regulatory standards. Collaboration with researchers for study design and team training is key.
Responsibilities
- Oversees and coordinates complex or multi-site clinical research studies for two clinical researchers.
- Serves as a resource to provide comprehensive information to clinical research staff promoting a smooth operation, preparation of regulatory compliance, and interaction with other departments.
- Acts as the primary liaison to PI in developing plans for research projects and discussing the interpretation of results.
- Designs, implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies.
- Provides guidance to members of research team in the implementation and evaluation of clinical research; trains new staff.
Requirements
- Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
- Clinical Research (3 Years)
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements). BLS certification must be obtained within one month of hire date.
- Skills: Supervision, Clinical Research Management, Clinical Study Protocols, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS)
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development opportunities
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