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Clinical Research RN Coordinator - Clinical Research Institute Non-Uni

Job in Arcadia, Los Angeles County, California, 91006, USA
Listing for: Keck Medicine of USC
Full Time position
Listed on 2026-03-11
Job specializations:
  • Healthcare
    Healthcare Nursing
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research RN Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Uni[...]

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.

Qualifications

& Requirements

Minimum Education:

Bachelor’s Degree Nursing

Minimum Experience:

5 years Clinical research nursing experience.

Minimum

Skills:

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.

Required

Certifications:

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.

Preferred Experience:

2 years Clinical nursing experience (ICU, CCU, MICU referred)

Preferred

Certifications:

CCRC (Certified Clinical Research Coordinator) certification from ACRP.

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