Clinical Research Assistant
- Assists research personnel with multiple research projects
- Pre-screens for eligible subjects for assigned studies based on written, broad eligibility criteria.
- Obtains consent from patients who will participate in non-interventional registry and observational studies, as well as some select, minimal risk device studies.
- Documents the informed consent process.
- Reviews eligibility criteria with the Principal Investigator and Clinical Research Coordinators/Nurses.
- Assists with enrollment and randomization of subjects.
- Assists with the coordination of research visits.
- Reviews study specific lab manuals and obtains and processes lab specimens, as required by the specified research protocol.
- Performs data entry by transcribing data from the source to the case report form (paper or electronic) and redacts source documents as requested.
- Serves as a liaison between research staff and the departments in which research is conducted.
- Performs other duties as assigned
- Bachelor’s degree in field related to science or health care.
- Current certification in phlebotomy is preferred.
- Knowledge of medical terminology.
- Knowledge of principles and techniques used in clinical research preferred.
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