• Director, Patient Services and HUB

    Sumitomo Pharma (Boston, MA)
    …+ Partner with Access Marketing, Brand, Data & Analytics, Legal, Compliance, Medical Affairs , IT, and other cross-functional teams to ensure alignment and ... role in optimizing patient access, affordability, and adherence through data -driven insights, digital innovation, and cross-functional collaboration. This position… more
    Sumitomo Pharma (08/15/25)
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  • Sponsored Projects Manager, Contracts

    Intermountain Health (Boston, MA)
    …Experience in Microsoft Office + Five (5) years of experience in clinical research, regulatory affairs , research finance + Bachelor's Degree in a clinical or ... and guidelines for the research administration area. + Maintains comprehensive data dashboards to monitor activity, generate reports for leadership review, and… more
    Intermountain Health (09/05/25)
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  • Clinical Research Director, Immunology…

    Sanofi Group (Cambridge, MA)
    …team and internal partners, such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing + ... (such as new drug application) and timely response to regulatory reviews) + Serve as a medical ...keep updated with the pre-clinical, clinical pharmacology and clinical data relevant to the molecule of interest and the… more
    Sanofi Group (09/04/25)
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  • Head of Privacy, SpeCare and North America

    Sanofi Group (Cambridge, MA)
    …world. In this role you will act as a global leader and expert on Data Privacy, promote and shape a culture of privacy, mastering TRT (Thoughtful Risk Taking) and ... a data subject centric approach. Reporting to our Chief Privacy...generate deeper insights to our Research, Marketing, commercial and medical activities. + Actively monitor North American privacy regulations/enforcements,… more
    Sanofi Group (07/16/25)
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  • Clinical Research Director

    Sanofi Group (Cambridge, MA)
    …team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing. + ... Review documents supporting clinical development such as Investigator's brochure, regulatory documents for IND/CTA, clinical sections of integrated development… more
    Sanofi Group (08/22/25)
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  • Clinical Research Director, I and I, Pulmonology

    Sanofi Group (Cambridge, MA)
    …team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing + ... Review documents supporting clinical development such as Investigator's brochure, regulatory documents for IND/CTA, clinical sections of integrated development… more
    Sanofi Group (08/30/25)
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  • Senior Counsel

    Fujifilm (Boston, MA)
    …Secretary, the Senior Counsel, will be responsible for handling all legal affairs relating to the ink and chemicals manufacturing businesses and the corporate ... across the industries we touch-from healthcare and photography to semiconductors and data storage. With roots in photosensitive materials and a legacy of… more
    Fujifilm (08/13/25)
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  • Senior Manager of Statistics- CMC

    Takeda Pharmaceuticals (Cambridge, MA)
    …and biomarker assay development and validation. + Collaborate with Global Manufacturing, Regulatory Affairs , and Global Quality to explore methods and implement ... analysis, and interpretation of Chemicals, Manufacturing, and Controls (CMC) study data throughout Pharmaceutical Sciences. We seek an innovative and inquisitive… more
    Takeda Pharmaceuticals (09/03/25)
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  • Associate Vice President, Companion Diagnostics

    Merck (Boston, MA)
    …immunology, neurology, cardiometabolic and others as needed by the pipeline. + Work with Regulatory Affairs to ensure that regulatory documents (eg, IDEs, ... stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role requires overseeing CDx development,… more
    Merck (09/03/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines,… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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