Research Coordinator III - Quantitative Health Sciences
Cleveland Clinic Main Campus, United States
USD 63K-69K (estimate) Senior-level Full Time
Tasks
- Assist in protocol development
- Communicate with research personnel
- Complete regulatory documentation
- Conduct informed consent
- Contribute to research budgets
- Coordinate study activities
- Develop research tools
- Maintain personnel certifications
- Maintain research data quality
- Manage clinical trials
- Monitor study progress
- Oversee regulatory compliance
- Prepare for audits
- Report adverse events
- Support study design and protocol development
Perks/Benefits
Skills/Tech-stack
Clinical Research | Communication skills | Computer Skills | Data Management | Database Management | GCP guidelines | IRB processes | Protocol development | Regulatory Compliance | Research protocol development | Spreadsheet software | Study coordination
Education
Roles
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