Clinical Research Nurse II
About The Position
The Clinical Trials Unit is seeking a Clinical Research Nurse II who will perform the following essential duties and responsibilities: Coordinate the implementation of clinical research projects. Organize the clinical research team and serve as an advocate for study subjects. Develop a recruitment plan for each assigned protocol with the research team. Identify potential sources for subjects and establish appropriate networks to support referrals. Conduct/monitor the screening and recruitment of subjects for research trials using knowledge of current protocols and inclusion/exclusion criteria to determine subject eligibility. Educate subjects on protocol related procedures/assessments in which they must participate as a study subject. Collect, organize, and maintain data and test results for source documentation of all research subjects. Write orders and administer medication/devices for the clinical care of research subjects. Assist in the management of the study subjects' health status during the course of research care and development of treatment plan related to the research protocol. Conduct any needed physical assessments using protocols for review by the Principal Investigator when appropriate.
Requirements
- Bachelor's degree in Nursing
- Current Kentucky license
- Two (2) years of related research or nursing experience
- If not ACRP or SoCRA certified should obtain the certification within the first three years.
Responsibilities
- Coordinate the implementation of clinical research projects.
- Organize the clinical research team and serve as an advocate for study subjects.
- Develop a recruitment plan for each assigned protocol with the research team.
- Identify potential sources for subjects and establish appropriate networks to support referrals.
- Conduct/monitor the screening and recruitment of subjects for research trials using knowledge of current protocols and inclusion/exclusion criteria to determine subject eligibility.
- Educate subjects on protocol related procedures/assessments in which they must participate as a study subject.
- Collect, organize, and maintain data and test results for source documentation of all research subjects.
- Write orders and administer medication/devices for the clinical care of research subjects.
- Assist in the management of the study subjects' health status during the course of research care and development of treatment plan related to the research protocol.
- Conduct any needed physical assessments using protocols for review by the Principal Investigator when appropriate.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
