About the role
Coordinate studies.
- Schedule
- Regular Full-Time
Read the full employer description →Read more
- Coordinate studies. This can involve startup work, regulatory activities, study management throughout the study, screening, consenting and enrolling patients, managing data flow, coordinating documentation and data storage, coordinating prehospital and hospital data flow, reviewing timeliness and prioritization needs with the study team to facilitate adherence to study-related benchmarks. - Review medical records, abstracting relevant variables into electronic systems.
Complete enrollment forms for both registry and trial patients. Also includes Pre-Hospital and Hospital data abstraction as needed, entry, and tracking using the local and web-based study databases. - Protocol compliance, QA/QC, study documentation - Ensure adherence to research protocol and...
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