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Clinical Research Coordinator II
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Full-time
- Coordinate the day-to-day administrative activities of gynecological oncology clinical research trial programs.
- Work with Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program.
- Assure compliance with all relevant IRB and other regulatory agency requirements.
- Prepare IRB documents and reports.
- Evaluate and write of research protocols in collaboration with the study investigator.
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