Case Report Form (CRF), Clinical Research, Data Entry, IR (Infrared), Intensive Care, Laboratory Testing, Maintain Compliance, Test Plan/Schedule, Time Management
- Screen and evaluate potential study participants for eligibility.
- Complete and maintain case report forms and participant binders, ensuring consents are current.
- Enter study data into the electronic database accurately and in a timely manner.
- Monitor patients throughout the clinical pathway (trauma, OR, IR, ICU, clinic) to ensure protocol adherence.
- Notify Trauma Research Manager of any protocol issues or concerns.
- Coordinate required lab testing and scheduling with Banner lab in collaboration with the Trauma Research Manager.
- Attend site visits and contribute to additional duties or projects as assigned.
- Explain the study, obtain consent, and enroll participants.
Knowledge, Skills & Ability:
- Ability to perform duties under minimal supervision with general expectations.