What are the responsibilities and job description for the Clinical Research Nurse position at ClinLab Staffing?
- Perform clinical functions i.e. phlebotomy, monitoring vital signs of study participants, etc., when warranted; educate family and contribute to the care and evaluation of subjects, including determining preliminary inclusion/ exclusion criteria.
- Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research participant scheduling, coordinate protocol-related research procedures, study visits, and follow—up, collect patient/ research participant history, collect, and maintain source documentation, perform data entry and query resolution, prepare IRB submissions, update required modifications, continuing reviews, and reportable events.
- Under the supervision of an investigator, conduct health assessments as medically necessary or required per protocol to assess or resolve adverse events, safety, and general health of study participants.
- Monitor study participants for adverse events and report any adverse events to the principal investigator, and study coordinator, if applicable.
- Administer study interventions and treatments as directed by the principal investigator, if appropriate for scope of license.
- Prepare and monitor administration, usage, and documentation of investigational products and other required treatments in clinical trials.
- Current LPN licensure in the state of employment.
Associate Degree in Nursing from an accredited school of nursing.
- BLS required
- Three years prior experience in a health-related clinic or research setting
- Proficient in the use of Microsoft Office applications
- Understanding of medical terminology
