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n Clinical Research Coordinator - Radiological Sciencesn
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n General Informationn
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n Work Location: Los Angeles, CA, USAn
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n Onsite or Remoten
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n Flexible Hybridn
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n Work Schedulen
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n Monday-Friday 8am-5pmn
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n Posted Daten
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n 05/28/2026n
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n Salary Range: $36.37 - 58.52 Hourlyn
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n Employment Typen
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n 2 - Staff: Careern
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n Durationn
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n Indefiniten
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n Job #n
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n 30856n
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n Primary Duties and Responsibilitiesn
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n Life-saving breakthroughs, innovative therapies, and next-generation technologies. Through vision, tenacity, and inspiration, UCLA Healthxe2x80x99s world-class researchers are redefining human health and patient care. Join us and live out your passion for discovery while making an incredible difference in the lives of people around the world.
The Study Coordinator supports the full operational lifecycle of clinical research studiesxe2x80x94from initial design and startxe2x80x91up through conduct and closeout. This role is responsible for implementing study activities for one or more protocols, managing dayxe2x80x91toxe2x80x91day tasks, and prioritizing work to meet project deadlines. The incumbent ensures strict adherence to study protocols, institutional policies, FDA regulations (CFR), and ICH Good Clinical Practice (GCP) standards.
Salary: $36.37 - $58.52 hourly
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n Job Qualificationsn
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Required:
Bachelors Degree
Minimum 3 years of related experience or training
Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.
Working knowledge of Institutional Review Board review and reporting requirements, institutional committee application and approval process, Contracts and Grants and departmental policies and procedures.
Working knowledge of Institutional Review Board and Internal Scientific Peer Review Committee. Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
Working knowledge of FDA Code of Federal Regulations and ICH good clinical practices for clinical research.
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As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer.
Current/former UC employees are subject to a personnel file review.
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