Clinical Research RN Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Exempt)
About The Position
The Clinical Research RN Coordinator position works collaboratively with investigator(s) and with formulating clinical research objectives, contributes to the design of clinical research protocols, oversees clinical research trials, and conducts quality assurance reviews. This position also addresses/resolves clinical trial patient complaints and schedules/coordinates/performs testing and/or treatments according to established protocols or as prescribed by a physician or principal investigator. Pay Transparency The hourly rate range for this position is $49.86 - $76.69. When extending an offer of employment, the University of Southern California Arcadia Hospital considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate’s work experience, education/training, key skills, internal peer equity, federal, State, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.
Requirements
- Bachelor’s Degree Nursing
- 5 years Clinical research nursing experience.
- Knowledge of research nursing practices, clinical expertise, and research compliance.
- Experience in conducting clinical research trials.
- Demonstrated commitment to quality service and care, teamwork, and hospital goals.
- Registered Nurse - RN (CA Board of Registered Nursing)
- Basic Life Support (BLS) Provided by the American Heart Association
- Health Insurance Portability and Accountability Act (HIPAA) Course Certification from CITI Program
- Human Subjects Research (HSR) Training Certification from CITI Program
- Good Clinical Practice (GCP) Training Certification from CITI Program
Nice To Haves
- 2 years Clinical nursing experience (ICU, CCU, MICU referred)
- CCRC (Certified Clinical Research Coordinator) certification from ACRP.
Responsibilities
- Works collaboratively with investigator(s)
- Formulating clinical research objectives
- Contributes to the design of clinical research protocols
- Oversees clinical research trials
- Conducts quality assurance reviews
- Addresses/resolves clinical trial patient complaints
- Schedules/coordinates/performs testing and/or treatments according to established protocols or as prescribed by a physician or principal investigator
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
