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Clinical Research Coordinator 1
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- Clinical Research Coordinator 1
- Perform specific protocol procedures such as scheduling study visits and procedures, interviewing subjects, collecting and processing study specimens, taking vital signs, collecting study ECG’s, etc.
- Understands study protocols and ensures all team members adhere to protocol specific procedures for patient safety and data quality assurance.
- Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
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