• Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (Boston, MA)
    …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... to medical safety of clinical trials, including monitoring of clinical trial safety and laboratory data. + Generates safety queries, evaluates safety data… more
    Sumitomo Pharma (08/15/25)
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  • Associate Manager, Data Validation Engineer

    Takeda Pharmaceuticals (Boston, MA)
    …following duties: provide strategic planning, integrating, execution, build and oversight of clinical trial deliverables. Program study level clinical data ... data cleaning and reconciliation and work cross-functionally with all members of Clinical Study teams to foster an environment of quality and efficient… more
    Takeda Pharmaceuticals (07/12/25)
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  • Associate Director, Global Health Economics Lead,…

    Takeda Pharmaceuticals (Boston, MA)
    …to cross-functional business partners about the need for additional data generation - clinical trial , real world evidence (RWE) such as registries and databases ... strategies for Health Technology Appraisal (HTA; including the EU Joint Clinical Assessment [JCA]) and payer assessments to optimize rapid, broad patient… more
    Takeda Pharmaceuticals (07/01/25)
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  • Manager, Global Trade Compliance

    Takeda Pharmaceuticals (Boston, MA)
    …of export and import compliance policies and procedures for the organization regarding Clinical Trial Material (CTM) and raw material shipments. + Manage daily ... Ensure adherence to country specific standard operating procedures for importing/exporting clinical trial material and raw materials, including logistics,… more
    Takeda Pharmaceuticals (06/08/25)
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  • The Head of EGDS Innovation and Center…

    Sanofi Group (Cambridge, MA)
    …development including diversity in clinical trials, digital biomarkers, and novel clinical trial designs + Drive development and scaling of advanced ... and market entry. For example, champion statistical innovation and novel clinical trial designs aligned with R&D priorities (eg, Proof of Mechanism/Proof of… more
    Sanofi Group (06/05/25)
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  • Contract Associate II

    Beth Israel Lahey Health (Boston, MA)
    …of paperwork related to the following agreements; confidentiality agreements (CDA), clinical trial agreements (CTA), subcontracts (Subs), amendments (Amendments) ... who will handle tasks of limited complexity to support and manage the Clinical Trials Office's role in clinical research contracting under its processes.… more
    Beth Israel Lahey Health (07/31/25)
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  • Senior Statistical Programmer FSP

    Cytel (Boston, MA)
    …spanning all therapeutic areas. + Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS ... Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or… more
    Cytel (07/24/25)
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  • Associate Director, Scientific Communications…

    Takeda Pharmaceuticals (Boston, MA)
    …Understanding of pharmaceutical clinical development and product life-cycle management, clinical trial design and execution, statistical methods and ... clinical clinical trial data reporting requirements + Experience in medical communications function, which may include publications, medical information,… more
    Takeda Pharmaceuticals (07/02/25)
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  • Senior Statistical Programmer FSP

    Cytel (Cambridge, MA)
    …**How you will contribute:** + Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS ... Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or… more
    Cytel (08/02/25)
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  • PRN Principal Investigator - Endocrinologist

    System One (Burlington, MA)
    …events, and medical histories + Consult with patients and caregivers to address clinical trial participation, safety, and related concerns + Maintain timely, ... serve as a PRN Principal Investigator (PI) for a clinical research site in Massachusetts. This is a hybrid...professional communication with all stakeholders to ensure trial continuity and data integrity Requirements + MD with… more
    System One (07/18/25)
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