Clinical Research Assistant
- Assist in data management, regulatory paper works and other local administrative tasks as supervised by the clinical research coordinator
- Coordinate research and administrative activities, ensuring all projects are completed according to project/study timelines
- Assist in the development of project/study policies and procedures. Administer policies and procedures according to protocol, Institutional Review Board (IRB), grant/contract and study and site specifications
- Recruit study participants and complete structured clinical assessments with participants
- Monitor and promptly respond to participant queries
- Collect and track study data and compile data reports
- Submit and maintain proper study records, including submission of timely reports to Institutional Review Boards
- Produce special and recurring reports
- Excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors and sponsors
- Knowledge of medical terminology
- Knowledge of good clinical practice, FDA, OHRP, HIPAA policies
- Familiarity with the Microsoft Office Suite
- Previous work with CRFs and EDC
- Excellent organizational skills to independently manage work flow
- Ability to prioritize quickly and appropriately
- Ability to multi-task
- Meticulous attention to detail
- Licensed candidates must have an Associate's degree and RN or LPN licensure
- One year of experience working in clinical research is preferred
- Psychology background preferred
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