• 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 ... and transform the lives of patients while transforming your career. Clinical Research Medical Director, Uplizna **What you will do** Let's do this. Let's change the… more
    Amgen (08/14/25)
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  • Clinical Research Coordinator - Cancer Center…

    Rush University Medical Center (Chicago, IL)
    **Job Description** Location: Aurora, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Cancer Center-Res Fac ... training period, this position will be located in Aurora, IL at Rush Copley Medical Center. Training will take place on-site at the Chicago, IL Rush University … more
    Rush University Medical Center (08/19/25)
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  • Associate Director, Product Quality

    AbbVie (Waltham, MA)
    …Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs , R&D, and S&T to ensure alignment on strategic ... Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs , Research and Development. Additional Information Applicable… more
    AbbVie (07/11/25)
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  • Medical Analytics, Care Gaps & Customer…

    Pfizer (Collegeville, PA)
    …users. + Plan, generate and perform asset-specific care gap analyses to guide Medical Affairs activities using advanced techniques such as predictive models, ... & Segmentation Team Leader in strategic and tactical planning with regards to medical analyses. + Collaborate with Care Gaps & Segmentation Team Leader to… more
    Pfizer (09/11/25)
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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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  • Principal Engineer, New Product Introduction

    Terumo Medical Corporation (Elkton, MD)
    …Management Office (PMO), Product Development, Process Development, Quality, Marketing, Regulatory Affairs , Operations, Supply Chain, Logistics and Distribution ... Sep 11, 2025 Req ID: 4976 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: PM&PD Management Terumo Medical Corporation (TMC) develops,… more
    Terumo Medical Corporation (08/13/25)
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  • Executive Director, Digital

    Gilead Sciences, Inc. (Foster City, CA)
    …not only be responsible for delivering best-in-class digital engagement within Public Affairs , but also transform the function into a modern, proactive, insight-led ... development and execution of a global digital communications strategy within Public Affairs , aligning with enterprise brand and business goals. Define the right mix… more
    Gilead Sciences, Inc. (09/03/25)
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  • Senior Clinical Director Ambulatory

    Penn Medicine (Philadelphia, PA)
    …continuing education and skill validation of clinical staff. Quality, Patient Safety, and Regulatory Affairs : Partnership with the Vice Chair for Quality, ... alignment with Health System Requirements. In conjunction with the Vice-Chair of Regulatory Affairs , develop programs that enhance the clinical decision-making,… more
    Penn Medicine (08/07/25)
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  • Senior Director, Global Strategic Marketing

    Abbott (Princeton, NJ)
    …of customer insights to identify product differentiation; partner with Market Access, Medical Affairs and Market insights to differentiate products with a ... roadmap to fill gaps + Partner with R&D, Clinical Affairs , Regulatory , Quality and Operations to ensure...pricing strategy for APOC product portfolio + Partner with Medical Affairs to define clinical evidence required… more
    Abbott (09/13/25)
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  • Reagent Labeling Writer Intern

    Danaher Corporation (Miami, FL)
    …degree in a relevant field such as Technical Communication, Professional Writing, English, Regulatory Affairs , or a related discipline. . 0-2+ years experience ... hands-on experience and exposure in the critical area of regulatory labeling within the medical device and...or coursework in technical writing, regulatory affairs , or scientific communication. . Proficiency… more
    Danaher Corporation (08/26/25)
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