Clinical Research Enrollment Assistant
Tasks
- Attend training sessions
- Collect participant demographic history
- Collect participant medical history
- Collect participant psychiatric history
- Collect urine samples
- Collect vital signs
- Confirm visit appointments
- Coordinate medication dispensation
- Enter data into electronic data capture
- Flag data inconsistencies
- Identify eligible participants
- Maintain compliance with ICH GCP
- Maintain source documentation
- Maintain study logs
- Maintain study trackers
- Perform HbA1c tests
- Perform phlebotomy
- Prepare informed consent materials
- Prepare participant files
- Print study paperwork
- Review study protocols
- Schedule participant visits
- Send visit reminders
- Support participant flow
Perks/Benefits
- 401k matching
- Dental insurance
- Employee assistance program
- Flexible spending account
- Health savings account
- Life insurance
- Medical insurance
- Paid time off
- Parental leave
- Professional development assistance
- Vision insurance
Skills/Tech-stack
Clinical trial | Clinical trial protocols | Data Capture | Data Management | Data entry | Drug screening | EDC | Electronic Data | Electronic data capture | HbA1c | ICH GCP | Informed consent | Medication dispensing | Microsoft Office | Participant Screening | Phlebotomy | Regulatory Compliance | Source Documentation | Trial Protocols | Urine Drug Screening | Vital signs
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