• Senior Corporate Counsel - Product Support

    Genentech (South San Francisco, CA)
    …strategies; + Advising on transactions to support external collaborations and partnerships; + Advising regulatory , medical affairs , and other clients on FDA ... advice and support across the lifecycle of Genentech's products, including commercial, medical affairs , market access, and government affairs . Supported… more
    Genentech (09/06/25)
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  • Medical Strategic Account Director, West…

    Sanofi Group (Portland, OR)
    …Biochemistry, Molecular Biology, Medicine) + Minimum of 3 years' experience in relevant Medical Affairs , Medical Science Liaison, or Therapeutic Area ... projects + Ability to work effectively with cross-functional teams, including commercial, medical , and regulatory , to achieve shared goals + Robust network… more
    Sanofi Group (09/13/25)
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  • Senior Medical Staff Coordinator…

    Henry Ford Health System (Wyandotte, MI)
    …problem-solving skills. Additional Information + Organization: Henry Ford Wyandotte Hospital + Department: Medical Affairs Office - WH + Shift: Day Job + Union ... . Assists the Manager in keeping current with all accreditation standards and regulatory requirements and education of the medical staff. Assist Manager in… more
    Henry Ford Health System (09/10/25)
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  • Director, Scientific Expert CMC

    Boehringer Ingelheim (Athens, GA)
    …new product and marketed product regulatory strategy in the Global Regulatory Affairs (RA) Chemistry, Manufacturing and Controls (CMC) function for ... with regulatory standards governing BIAH products and processes. + Represents regulatory affairs as a key leader during manufacturing site inspections,… more
    Boehringer Ingelheim (09/12/25)
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  • Senior Manager, Clinical Science

    Abbott (Plymouth, MN)
    …cross-functional teams, including Marketing, R&D, Field Operations, Risk Management, Reimbursement, Medical Affairs , Quality, and Regulatory Affairs ... at multiple levels in the organization. + Familiarity with relevant international regulatory requirements for medical devices including Quality Systems standards… more
    Abbott (08/14/25)
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  • Quality/Pt Safety Advisor

    Vanderbilt University Medical Center (Nashville, TN)
    **Discover Vanderbilt University Medical Center** : Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, ... quality improvement advisor to provide project management facilitation, education, and data analysis for improvement of systems and processes, under occasional… more
    Vanderbilt University Medical Center (09/09/25)
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  • Clinical Research Medical Director- Uplizna

    Amgen (Washington, DC)
    …global strategy + Support cross-functional and global collaborations to integrate broad medical , regulatory , safety, scientific, and commercial access, and value ... safety and regulatory interactions. + Interpret and communicate clinical trial data . + Author/review CSRs, publications, and regulatory submissions + Develop… more
    Amgen (08/14/25)
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  • Head of Safety and Pharmacovigilance - Cell…

    Gilead Sciences, Inc. (Foster City, CA)
    …signal detection and decision-making. **Cross-Functional Collaboration** * Partner with Clinical Development, Regulatory Affairs , Medical Affairs , and ... even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People… more
    Gilead Sciences, Inc. (09/09/25)
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  • Medical Coder Inpatient

    University of Michigan (Ann Arbor, MI)
    …ensure completeness, accuracy and compliance with established guidelines of all governmental regulatory agencies and third-party payers. + Reviews medical record ... Medical Coder Inpatient Apply Now **Job Summary** Advanced...Group, (APR-DRG) based on payor classification and abstracts specific data elements for each case in compliance with federal… more
    University of Michigan (09/06/25)
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  • Medical Device Complaint Handling…

    ThermoFisher Scientific (Middletown, VA)
    … requirements + Collaborate with cross-functional teams, including Quality Assurance, Regulatory Affairs , and Product Development, to resolve complaints. + ... VA Specialty Diagnostics Group (SDG) **How will you make an impact?** The Medical Device Complaint Handling Specialist III is responsible for managing and resolving… more
    ThermoFisher Scientific (08/31/25)
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