• Associate Director, Complaint Handling

    Abbott (Alameda, CA)
    Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in… more
    Abbott (07/01/25)
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  • Head of Clinical Development - JAPAC

    AbbVie (North Chicago, IL)
    …preferred. + Broad knowledge of drug development, clinical operations, and on-market medical affairs . + Demonstrated high-level of competency in the AbbVie ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...development strategy for the JAPAC region in alignment with global strategies. This includes assessing regional needs and translating… more
    AbbVie (08/28/25)
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  • Oncology Early Stage Clinical Scientist (Director,…

    Pfizer (South San Francisco, CA)
    …(POC) studies in Oncology. You will work in close collaboration with the Global Development Lead (GDL)and members of the development team to establish, lead, ... Medicine, and Digital Medicine). **POSITION RESPONSIBILITIES** + Partner closely with the Global Development Lead (GDL) in the execution of the clinical development… more
    Pfizer (08/21/25)
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  • Sr. Director Clinical Development - Lilly Gene…

    Lilly (Indianapolis, IN)
    …provide insight into clinical development programs both externally and internally (eg, Medical Affairs , Commercial, CROs, etc.). They will provide clinical / ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
    Lilly (08/08/25)
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  • Associate Director, Clinical and Safety Quality…

    Takeda Pharmaceuticals (Boston, MA)
    …of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, ... teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and determined by compliance… more
    Takeda Pharmaceuticals (07/25/25)
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  • Associate Director, PV Vendor Management Team…

    Ascendis Pharma (Palo Alto, CA)
    …for the targeted audience (as needed) + Functions as a PV advisor to Medical Affairs , Commercial Organizations and other relevant stakeholders as applicable. + ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled,… more
    Ascendis Pharma (07/19/25)
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  • Tier 2, Technical Support Representative

    IQVIA (Des Moines, IA)
    …patient support, field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more ... - Location (Open to Remote US)_ As the only global provider of commercial solutions, IQVIA understands what it...to deliver nationally and internationally. Our teams help biopharma, medical device and diagnostic companies get their therapies to… more
    IQVIA (09/20/25)
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  • Associate Director, Regulatory Policy

    Bristol Myers Squibb (Bethesda, MD)
    …team, the Associate Director Regulatory Policy brings an expertise in regulatory affairs and related policy. The Associate Director, Regulatory Policy is responsible ... and actionable outcomes. The incumbent acts as a critical link between global , regional, and local regulatory environments, ensuring the business stays ahead of… more
    Bristol Myers Squibb (09/25/25)
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  • Associate Director, Product Source Management

    Merck (West Point, PA)
    …diversity, and effectiveness . Regulatory Acumen and effective working relationship with Global Regulatory Affairs and Clinical Safety (GRACS) . Demonstrated ... . Managing multiple projects at any one time that have high complexity ( global supply chain impact with many inter dependencies) . Leading and executing within… more
    Merck (09/24/25)
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  • Principal Scientist, Translational Research / CDx

    Merck (Boston, MA)
    …Company, collaborating with project teams, biomarker leads, clinical operations, and regulatory affairs on the implementation of global CDx assay strategies in ... pre-submissions, briefing books, IDEs, IVDR PSAs, PMAs. + Participate in meetings with global regulatory agencies to provide CDx expertise. + Provide CDx input into… more
    Merck (09/22/25)
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