Clinical Research RN Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Exempt) Job at University of Southern California, Arcadia, CA

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  • University of Southern California
  • Arcadia, CA

Job Description

JOB QUALIFICATIONS:

Education
Required: Bachelor's Degree Nursing

Work Experience

Required:
X 5 years Clinical research nursing experience.
X 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
Required:
- 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

MThe 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 finding, 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.

USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.

We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at [click to reveal phone number](213) 821-8100 , or by email at [click to reveal email address] uschr@usc.edu . Inquiries will be treated as confidential to the extent permitted by law.

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If you are a current USC employee, please apply to this USC job posting in Workday by copying and pasting this link into your browser:
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Job Tags

Hourly pay, Full time, Work experience placement, Local area,

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