• Oncology Scientific Communications Team Lead (Sr.…

    Pfizer (Cambridge, MA)
    …alignment with the SCP. + Deliver internal communications around new scientific and clinical data on medicines and disease areas of interest, coordinating ... TA teams to manage the publication planning, writing, and dissemination of scientific data from clinical trials and research activities, ensuring a cohesive and… more
    Pfizer (10/17/25)
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  • Senior Project Biostatistics Lead- Vaccines

    Sanofi Group (Waltham, MA)
    …challenges** + (S)He interacts with other GBS teams, Clinical , Regulatory, Global Program Head, Regulatory, Immunology, Medical Writing, Data Management + ... Expert at vaccine project level: + Develop with other clinical /medical and global project team members the...support the label claims + ensure quality of the clinical data CDISC packages are delivered and… more
    Sanofi Group (09/17/25)
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  • Associate Director, Regulatory Affairs (Oncology)

    Sumitomo Pharma (Boston, MA)
    clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data ) and contributes ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data )… more
    Sumitomo Pharma (10/11/25)
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  • Biostatistics Lead, Next Generation Immunology

    Sanofi Group (Cambridge, MA)
    …and written communication skills + Relevant disease area knowledge working directly on clinical trial protocols and data reporting in industry setting + ... experience designing and/or conducting statistical analyses from human Phase 3 or 4 clinical trial data , either pre-planned and post-hoc OR + Master's degree… more
    Sanofi Group (10/18/25)
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  • Associate Director, R&D Quality Governance

    Bristol Myers Squibb (Devens, MA)
    … and pharmacovigilance functions that empowers decision-making through data -driven insights, cross-functional collaboration and continuous innovation. Ensuring that ... interrogation of data to derive meaningful, actionable insights that support data -driven decision-making at Global GxP Quality Councils. + Support CAPA… more
    Bristol Myers Squibb (10/15/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (Boston, MA)
    clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data ) and contributes ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data )… more
    Sumitomo Pharma (09/09/25)
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  • GRA Device Associate

    Sanofi Group (Cambridge, MA)
    …and clinical performance studies.Ability to synthesize and critically analyze data from multiple sources. + **Collaboration Skills:** Ability to work effectively ... information can be found through the LINK (https://benefits.sanofiusallwell.com/fleet/public/index/ba511bf8-5c32-4828-9861-ab985fffab90/?cid=sanofi) . Global Terms & Conditions and Data Privacy… more
    Sanofi Group (09/20/25)
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  • Associate Director, US Medical Neuroscience…

    Takeda Pharmaceuticals (Lexington, MA)
    …You will have tactical accountability grounded in science, disease state, and competitive clinical data in support of one or more products, and supports ... + Tactical accountability grounded in science, disease state, competitive clinical data in support of one or...the assigned TA and represent medical affairs at the Global level for a product/franchise. + Provide clinical more
    Takeda Pharmaceuticals (10/10/25)
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  • Senior Manager, Feasibility

    Takeda Pharmaceuticals (Boston, MA)
    … research setting at a sponsor or CRO. + 6+ years of experience in Clinical Operations, Data Analytics, global feasibility, and trial optimization with ... data -driven feasibility assessments for Phase I - IV clinical studies, including protocol design optimization, country/site feasibility and selection, enrollment… more
    Takeda Pharmaceuticals (10/14/25)
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  • Patient Recruitment & Retention Strategy Lead…

    ThermoFisher Scientific (Waltham, MA)
    clinical trials/indications across the client. This role will work with the global clinical team and leaders to understand patient recruitment needs at a ... Regulatory Compliance:** Ensure that all recruitment activities adhere to ethical standards , regulatory requirements and Good clinical Practice (GCP) guidelines.… more
    ThermoFisher Scientific (10/11/25)
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