• Director -Design Quality…

    Philips (Cambridge, MA)
    As a key member of the Philips Ultrasound Quality Organization, the Director of Design Quality Engineering will lead/develop a global Design Quality Engineering team ... Leader-Ultrasound, you will partner with R&D, Product Management, Medical Safety & Clinical and other key functions to ensure the safety, reliability and efficacy… more
    Philips (11/13/25)
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  • Managing Consultant/Associate Director

    Guidehouse (Boston, MA)
    …Authorized to work for any US employer without sponsorship. As an Associate Director + BA/BS degree in Science, Engineering, Healthcare, Business or related course ... Healthcare and Life Science industries. + Ability to grasp and communicate clinical and business implications of technically complex products and services. + Ability… more
    Guidehouse (11/12/25)
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  • Senior Director , Global Regulatory Lead…

    Takeda Pharmaceuticals (Boston, MA)
    …medicines and make a lasting impact on patients worldwide. Join Takeda as a Senior Director , Global Regulatory Lead - Oncology, where you will be part of the global ... regulatory insight on one or multiple complex global oncology projects in clinical development with focus on innovative ways of addressing barriers to development… more
    Takeda Pharmaceuticals (11/01/25)
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  • Senior Director , Global Program Leader…

    Takeda Pharmaceuticals (Boston, MA)
    …that will inspire you and empower you to shine? Join us as a Senior Director , Global Program Leader - Oncology, Solid Tumors in our Cambridge office. At Takeda, we ... global launch projects. + Links GPT cross-functional sub-teams, such as the Clinical Subteam, Commercial Subteam, Pharmaceutical Sciences (CMC) Subteam, etc. to the… more
    Takeda Pharmaceuticals (10/23/25)
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  • Director , Toxicology

    Editas Medicine (Cambridge, MA)
    …to patients with genetic disorders. Characterizing Your Impact: As the Director , Toxicology you will: + Develop phase-appropriate nonclinical safety strategies and ... budgets, and regulatory compliance + Deliver high-quality safety reports to support clinical plans and regulatory filing submissions in multiple markets + Serve as… more
    Editas Medicine (10/12/25)
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  • Medical Director , Gastrointestinal…

    Takeda Pharmaceuticals (Boston, MA)
    …+ Analyze and interpret safety data from various sources including non- clinical , clinical , post-marketing and scientific literature. + Conduct signal ... for critical documents (eg, protocols and amendments, ICFs, IBs, IMPDs, clinical research reports, Health Hazard Evaluations, Signal Evaluation Reports, INDs, NDAs,… more
    Takeda Pharmaceuticals (11/23/25)
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  • Associate Director , Statistics (Hybrid)

    Takeda Pharmaceuticals (Boston, MA)
    …(from statistics, programming, outcomes research and epidemiology, quantitative clinical pharmacology, digital strategy, library sciences and data ... with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality statistical analyses, and pursue… more
    Takeda Pharmaceuticals (09/20/25)
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  • Director , Safety Risk Lead (MD)

    Pfizer (Cambridge, MA)
    …Working with other Pfizer functions engaged in benefit-risk management (Regulatory, Quality, Clinical , Medical, Corporate Audit, etc) to enable one medical voice + ... and mentoring of the team as required. + Makes decisions based on clinical experience + Assesses the suitability of biopharmaceutical products on typical physician… more
    Pfizer (11/20/25)
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  • Administrative Director Division…

    Beth Israel Lahey Health (Boston, MA)
    …management, improvements in access, overall customer satisfaction, communication, clinical service delivery, operating efficiency, and staff development. **Job ... decisions. Appoints, develops, manages and evaluates administrative, practice and clinical managers in designated areas. 2. Ensures that department activities… more
    Beth Israel Lahey Health (10/30/25)
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  • Head of Global Research Quality (Sr…

    Takeda Pharmaceuticals (Boston, MA)
    …dedicated to ensuring integrity, compliance, and ethical excellence in non- clinical research activities, studies, and processes supporting Takeda's R&D pipeline. ... and effectively deploy resources to mitigate compliance risks for Research non- clinical studies conducted externally in non-OECD Mutual Acceptance of Data system… more
    Takeda Pharmaceuticals (10/16/25)
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