- Miami, Florida, United States
- Full-time · Entry
- 1+ years
Entry-level clinical research professional responsible for data management and implementation of simple clinical research protocols.
Responsibilities
- Performs chart review/pre-screening activities for study participant eligibility
- Coordinates routine activities of clinical studies including data collection and maintenance
- Schedules appointments and study visits
- Performs moderate to complex research tests
- Assists in observing and informing the PI/supervisor of adverse events
Requirements
- Bachelor’s degree in relevant field
Skills
Benefits
- Medical
- Dental
- Tuition remission