Clinical Research RN Coordinator - Clinical Research Institute Non-Uni

Job Qualifications

Education

• Required:
  
  Bachelor’s Degree Nursing

Work Experience

• Required:
  
  5 years Clinical research nursing experience
• 2 years Clinical nursing experience (ICU, CCU, MICU preferred)

Knowledge,

Skills and Abilities

• 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.

Licenses/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 Certification from CITI Program

Preferred:

• CCRC (Certified Clinical Research Coordinator) certification from ACRP.

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.

The Clinical Research RN Coordinator manages clinical trial patients and all study data collection. This position explains the study to patients and potential patients, and educates staff about clinical trials and processes. The Clinical Research RN Coordinator collaborates with investigator(s) and provides guidance with formulating clinical research objectives, contributes to the design of clinical research protocols, oversees clinical research trials, and conducts quality assurance reviews.

This position monitors patient’s status throughout the study, reviews and evaluates health status, lab findings, and reactions. May also address/resolve clinical trial patient complaints and schedule/coordinate/perform testing and/or treatments according to established protocols or as prescribed by a physician or principal investigator.

Job REQ

Posted Date 10/27/2025

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