• Associate Director, Biostatistics

    Pfizer (Cambridge, MA)
    …+ Is an individual contributor role who specializes in creating clinical study designs, performing data analysis, providing data interpretation, and contributing ... to clinical publication and regulatory submissions. + Provides statistical input...and data analysis * Programming skills in R and/or SAS * Company SOPs and business practices * Demonstrated… more
    Pfizer (01/08/26)
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  • Senior Biostatistician FSP

    Cytel (Cambridge, MA)
    **Who Are You?** An experienced Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will ... support or lead one or more Phase I-IV clinical studies. You are excited and enthusiastic. You motivate...reporting, regulatory questions etc. is a plus. + Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables,… more
    Cytel (12/21/25)
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  • Senior Project Biostatistics Lead- Vaccines

    Sanofi Group (Waltham, MA)
    …for medium complexity vaccine project (one or several indications) in clinical development and/or post-marketing stage. The incumbent is accountable for all ... statistical aspects of clinical development/medical affairs plans, studies and submissions activities (when...Ability to work in a team + Computer skills ( SAS , R, Office) **Why Choose Us?** + Bring the… more
    Sanofi Group (12/16/25)
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  • Associate Director, Biostatistics

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …responsible for providing statistical expertise/input in the drug development including clinical development plan and regulatory submission strategy. This is a ... in the development of protocols and statistical designs in different phases of the clinical trials leading to approval of drug products in different phases of the … more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Lead Biostatistician - FSP

    ThermoFisher Scientific (Cambridge, MA)
    …step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel ... frameworks for clinical research through our PPD clinical research... trials + You are proficient in statistical software ( SAS and/or R); + You are able to collaborate… more
    ThermoFisher Scientific (11/06/25)
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  • Sr Financial Data Analyst

    Baystate Health (Springfield, MA)
    …analysis,and forecasting + Utilizes software including Microsoft SQL Server and/or SAS to perform queriesutilizingthe data warehouse, to refresh financial models and ... data interpretation,analysisand reporting + Experience with both financial and clinical data, and complexities of models forvarious typesofprovidervalue basedrisk… more
    Baystate Health (01/08/26)
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  • Director, Outcomes Research & Data Science

    Takeda Pharmaceuticals (Cambridge, MA)
    …to the development and execution of US Medical strategies to elucidate unmet clinical , economic, and patient-centered needs and product value. * Executing studies in ... Proficiency in statistical software and data visualization tools (eg, SAS , R, Python) with at least 5 years of..., R, Python) with at least 5 years of SAS experience specifically in administrative claims data is required.… more
    Takeda Pharmaceuticals (12/06/25)
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  • Principal Biostatistician

    Edwards Lifesciences (Boston, MA)
    …you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality ... innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients...design, statistical modeling, and data analysis + Proficient in SAS ; experience with R, S-Plus + Thorough understanding of… more
    Edwards Lifesciences (12/12/25)
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  • Statistical Project Leader

    Sanofi Group (Cambridge, MA)
    …Director) to drive evidence generation across Phase IIIB & IV clinical trials, observational and prospective real-world evidence studies. You'll have opportunities ... (CROs, academic collaborators, DMCs) + Partner with Medical Affairs, Clinical Development biostatistics, Pharmacovigilance, Regulatory, HEOR, and other functions to… more
    Sanofi Group (12/20/25)
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  • Programming Project Leader

    Sanofi Group (Cambridge, MA)
    …standardization and consistency of documents and programming deliverables across studies ( clinical study reports, CSR) and for integrated analyses (ISS/ISE). + ... deliverables in both study and submission level activities. + Participates in clinical project meetings and provide input, whenever relevant. + Identifies areas for… more
    Sanofi Group (12/18/25)
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