Overview
Responsible for all aspects of research coordination for research studies; responsible for research specific quality nursing care for patients participating in clinical trials.
Responsibilities
Essential Functions
- Plan, implement and monitor participant recruitment and retention procedures.
- Screen and interview study participants.
- Maintain case report forms, charts and documentation.
- Review lab and procedure results.
- Dispense medication and maintain records.
- Perform procedures as needed.
- Assure that adverse events are reported in a timely fashion.
- Maintain Regulatory documents as mandated by FDA regulations.
- All other duties as assigned.
Qualifications
Experience Requirements
- 2 years Nursing or Certified Clinical Research Coordinator required or
- 4 year degree in health science related field with clinical research experience required.
Education Requirements
- High School Diploma or GED Equivalent required.
- Bachelors in Health Science related field required.
UFJPI is an Equal Opportunity Employer and Drug Free Workplace.
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