325 coding-"https:" "https:" "https:" "https:" "https:" "https:" "Data driven Materials Modeling" uni jobs at University of California, Los Angeles
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, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research
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standards applicable to healthcare facilities and state/local building and fire codes. Knowledge of building automation and control systems. Ability to read blueprints. Infection prevention and control
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, and Bluebeam, with the ability to learn and work with different software products and analyze data for management reporting. Preferred · Familiarity with California Building Code, Title 22
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, and durable medical equipment terminology. Familiarity with insurance authorization processes, payor requirements, medical billing practices, and coding systems including CPT, HCPCS
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with clinical billing (IDX codes) Knowledge of human anatomy and pathology Strong attention to detail and multi-tasking abilities You will be required to rotate to all radiology sites staffed by UCLA
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University of California, Los Angeles | Los Angeles, California | United States | about 2 months ago
-depth knowledge of physician and facility billing practices, CPT coding initiatives, ICD-10 coding standards, and revenue/HCPCS coding Understanding of provider network/IPA arrangements
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minimal supervision and complete assignments in a timely manner. Working knowledge of medical terminology. Working knowledge of ICD-10 sufficient to code medical diagnosis. Skill in telephone business
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University of California, Los Angeles | Los Angeles, California | United States | about 2 months ago
proficiency in data management and statistical programming languages (SAS, SQL, R, STATA, or Python) (Required) Deep familiarity with drug coding systems (NDC, ATC), diagnosis and procedure codes (ICD, CPT
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activities to ensure compliance with study protocols and applicable regulations, including institutional policies, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The role involves
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policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Study Coordinator collaborates with the Principal Investigator (PI), ancillary departments