• Medical Records Technician (Coder) In/Out

    Veterans Affairs, Veterans Health Administration (North Chicago, IL)
    …code to ensure ethical, accurate, and complete coding. Monitors ever-changing regulatory and policy requirements affecting coded information for the full spectrum ... influenza vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Complete all application requirements detailed in… more
    Veterans Affairs, Veterans Health Administration (10/16/25)
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  • Lead Health System Specialist

    Veterans Affairs, Veterans Health Administration (Chicago, IL)
    …provider exit reviews and assessments, privileging actions, and guidance related to clinical performance concerns. Team Leader Duties: Serves as lead specialist over ... Medical Staff Bylaws updates and revisions; interpret and explain new regulatory requirements and VHA requirements, procedures and processes and contribute to… more
    Veterans Affairs, Veterans Health Administration (10/30/25)
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  • EHRM Pharmacy Technician (Inventory Automation…

    Veterans Affairs, Veterans Health Administration (Hines, IL)
    …controlled substance inspection process, discrepancies and resolution. Attends regulatory meetings regarding all inventory/automation and supplies and provides ... influenza vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Complete all application requirements detailed in… more
    Veterans Affairs, Veterans Health Administration (11/01/25)
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  • Clinical Research Regulatory…

    Rush University Medical Center (Chicago, IL)
    …depending on the circumstances of each case. **Summary:** This positions provides regulatory support for multiple clinical research studies, which may involve ... report(s) for distribution to PI, Administrator, Office of Research Affairs , Sponsor and Compliance throughout the conduct of the...analysis documents. * Maintains accurate records related to the regulatory aspects of clinical research. * May… more
    Rush University Medical Center (08/28/25)
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  • Associate Medical Director/Scientific Director,…

    AbbVie (North Chicago, IL)
    …interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other ... to augment expertise in the therapeutic area. . Responsible for understanding the regulatory requirements related to the clinical studies and global drug… more
    AbbVie (10/30/25)
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  • Senior Manager, RA Global Regulatory…

    AbbVie (North Chicago, IL)
    …responses. Advise internal customers who may contribute to regulated communication on Regulatory /FDA issues including Public Affairs , Clinical Development, ... Description Responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or… more
    AbbVie (10/28/25)
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  • Home Health Facility Licensure & Regulatory…

    CenterWell (Springfield, IL)
    …Minimum of 5 years of experience in healthcare compliance, facility licensing, or regulatory affairs , preferably in home health. + Knowledge of CMS regulations, ... are seeking a detail-oriented and experienced Home Health Facility Licensure & Regulatory Compliance Analyst to join our team. The successful candidate will oversee… more
    CenterWell (10/30/25)
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  • Medical Director, Medical Device, Patient Safety

    AbbVie (North Chicago, IL)
    …in close collaboration with cross-functional teams and counterparts in quality systems, regulatory affairs , medical writing, clinical development, ... areas to identify, evaluate, and communicate safety issues. May contribute relevant clinical safety input to new product design teams as needed. The Medical… more
    AbbVie (10/26/25)
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  • Manager, Clinical Project Management

    Edwards Lifesciences (Chicago, IL)
    …our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for ... Clinical Project Management** , you will manage clinical trials activities and ensure all applicable regulatory... clinical trials activities and ensure all applicable regulatory requirements are met. This role requires the ability… more
    Edwards Lifesciences (10/21/25)
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  • Medical Director/Senior Medical Director,…

    AbbVie (North Chicago, IL)
    …interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other ... to the molecule and disease area; partners with Medical Affairs , Commercial and other functions in these activities as...in the therapeutic area. + Responsible for understanding the regulatory requirements related to the clinical studies… more
    AbbVie (10/09/25)
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