- Screens, recruits and consents study participants.
- Verifies eligibility, completes screening procedures, schedules and conducts study visits, collects and processes data collection, completes research related forms, completes electronic data entry and maintains study subject data.
- Instructs and counsels patients in research procedures, to include administration, monitoring, recording and analyzing data.
- Ensures compliance with all federal and local regulations.
- Monitors close-out of studies and ensures records are retained for appropriate length of time.
- Reviews goals and requirements of any new protocols; plans and designs source documentation for protocol; and coordinates study initiation.
- Coordinates and manages clinical research projects for Principal Investigator via study protocol including assessment, planning, evaluation and intervention for the well-being of study participants.
- Performs all other duties as assigned.
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Clinical Research Nurse Associate- Mays Cancer Center - San Antonio, United States - UT Health San Antonio
Description
Job Summary:
Under direct supervision, responsible for coordinating and participating in clinical research studies conducted by principal investigator, to include recruitment, collection, compilation, documentation and analysis of clinical research data.
Job Duties:
Education:
Associate's degree is required.
Experience:
One (1) year nursing experience in the designated study area is required.
Additional Licenses and Certifications:
Texas RN license is required.