Study Coordinator
- Monitor study activities to ensure compliance with protocol and with all relevant local, federal and state regulatory and institutional policies
- Perform and follow protocol procedures such as interviewing subjects obtaining informed consent forms, taking vital signs and performing electrocardiograms
- Participation in initiation visits/investigators for assigned clinical trails and implements these trails according to deadline schedule mutually agreed upon by PI and sponsor
- Follow protocols and physician orders
- Responsible for participant interviews, screening, recruitment and data collection
- Educated participants on studies and anticipated outcomes
- Schedule subjects for appointments and procedures as required by study protocols