• Medical Psychiatry Research Assistant(6…

    Stanford University (Stanford, CA)
    …other study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case report ... Medical Psychiatry Research Assistant(6 Month Fixed Term) **School...forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board… more
    Stanford University (08/07/25)
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  • Medical Billing Specialist II - Patient…

    Ventura County (Ventura, CA)
    …identify compliance and audit issues and work progressively with the compliance office to identify and resolve regulatory conflicts. + Communicate ... Medical Billing Specialist II - Patient Financial Services...processing claims appropriately for timeliness in reimbursement and billing compliance with Medi-Cal, Medicare, and general insurance reimbursement requirements.… more
    Ventura County (08/02/25)
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  • Lead Medical Radiation Physicist - Sharp…

    Sharp HealthCare (San Diego, CA)
    …program and record keeping techniques for on-going quality assurance and regulatory agency review .Responsible for inspecting and implementing all provisions ... tasks to meet the goals of quality, safety and regulatory requirements. This position may require travel to other...therapist to ensure adequate performance of their duties and review of the performance.Advises Administration and Medical more
    Sharp HealthCare (07/12/25)
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  • Behavioral Health Medical Director…

    Humana (Sacramento, CA)
    …site of service should be authorized. All work occurs within a context of regulatory compliance and work is assisted by diverse resources which may include ... quality of care, audit, grievance and appeal and policy review . The Behavioral Health Medical Director will...the policy of Humana to take affirmative action, in compliance with Section 503 of the Rehabilitation Act and… more
    Humana (08/09/25)
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  • Patient Care Technician - PCT Ccht - Dialysis

    Fresenius Medical Center (Murrieta, CA)
    medical records according to company policy and procedure and in compliance with all appropriate regulatory requirements + Maintains logs as directed ... nurse in accordance with organization policies, procedures, and training and in compliance with regulations set forth by the corporation, state, and federal… more
    Fresenius Medical Center (08/16/25)
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  • Sr. Medical Director, Clinical Development…

    Bristol Myers Squibb (San Diego, CA)
    …+ Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and regulatory documents + Conduct ... aims to be the global leader in radiopharmaceuticals . The Senior Medical Director - Clinical Development (GU Cancer/Prostate Renal) has responsibility for the… more
    Bristol Myers Squibb (07/08/25)
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  • Director, Safety Scientist

    BeOne Medicines (Emeryville, CA)
    …answer ad-hoc safety queries from ethics committees. + Lead the authoring and review of safety sections of regulatory submissions, eg, IND/CTA (General ... execution, communication and influence with internal stakeholders (eg, clinical development, medical , regulatory , labeling) and external stakeholders (eg FDA,… more
    BeOne Medicines (07/02/25)
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  • Patient Safety Specialist (Registered Nurse)…

    Cedars-Sinai (Marina Del Rey, CA)
    …+ One (1) to two (2) years of experience in quality improvement, regulatory compliance , or performance improvement, with a strong preference for candidates ... limited to Core Measures, Patient Safety Indicators (PSI-90), and Mortality review processes, to ensure sustained optimal performance. The Patient Safety Specialist… more
    Cedars-Sinai (07/30/25)
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  • Director, Medical Affairs Strategy…

    Sumitomo Pharma (Sacramento, CA)
    …Initiated Study and Collaborative Research program. + Provide detailed and compliant medical review and approval of external resources, communications, and ... track record of detailed, medically accurate, and scientifically relevant writing and review skills in line with compliance requirements. + Experience… more
    Sumitomo Pharma (07/30/25)
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  • Associate Director, Safety Scientist

    BeOne Medicines (San Mateo, CA)
    …answer ad-hoc safety queries from ethics committees + Lead the authoring and review of safety sections of regulatory submissions, eg, IND/CTA (General ... execution, communication and influence with internal stakeholders (eg, clinical development, medical , regulatory , labeling) and external stakeholders (eg FDA,… more
    BeOne Medicines (07/08/25)
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