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Form of workJob 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. Assists in the determination of guidelines for the collection of clinical data and/or administration of clinical studies.
Job Duties:
1. Screens, recruits and consents study participants.
2. 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.
3. Instructs and counsels patients in research procedures, to include administration, monitoring, recording and analyzing data.
4. Ensures compliance with all federal and local regulations.
5. Monitors close-out of studies and ensures records are retained for appropriate length of time.
6. Reviews goals and requirements of any new protocols; plans and designs source documentation for protocol; and coordinates study initiation.
7. 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.
8. Performs all other duties as assigned.
Education:
Associate's degree is required.
Experience:
One (1) year nursing experience in the designated study area is required. Experience in Women's Health, Ob-Gyn, or Oncology preferred.
Additional Licenses and Certifications:
Texas RN license is required.
Additional Skills:
Bilingual (English and Spanish) preferred.
