• Lead Clinical Programmer - FSP

    Parexel (Harrisburg, PA)
    **PXL is seeking a clinical operations lead with expertise in clinical sample logistics and proficiency in computational programming to support the generation ... development of tools and dashboards for sample/data tracking, review of clinical sample collection, resolving sample/data queries, and support of database lock… more
    Parexel (10/11/25)
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  • Senior Statistical Programmer - Analysis…

    Merck (North Wales, PA)
    …all our Company therapeutic areas except early oncology. The senior statistical programmer will gather and interpret user requirements for analysis and programming ... requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into… more
    Merck (11/07/25)
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  • Associate Principal Statistical Programmer

    Merck (North Wales, PA)
    …all our company therapeutic areas except early oncology. The Associate Principal Programmer will gather and interpret user requirements for analysis and programming ... requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into… more
    Merck (11/19/25)
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  • Senior Scientist, Statistical Programmer

    Merck (North Wales, PA)
    …all our company therapeutic areas except oncology. The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve ... listings and figures according to statistical/modeling analysis plan. The senior programmer will be a key collaborator with statisticians, modelers, and colleagues… more
    Merck (11/07/25)
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  • Principal Statistical Programmer

    IQVIA (Philadelphia, PA)
    …complex project or client requirements. **Job Details:** + Position: - Principal Statistical Programmer + Home Based + Min 7+ years of CRO/Pharma Industry + ... + Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data...ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes. + Minimum of 7+ years of… more
    IQVIA (11/05/25)
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  • Associate Principal Scientist, Statistical…

    Merck (North Wales, PA)
    …programming activities for multiple and/or late stage drug/vaccine clinical development projects. Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
    Merck (09/30/25)
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  • Sr. Scientist, Statistical Programmer

    Merck (North Wales, PA)
    …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
    Merck (09/05/25)
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  • Senior Statistical Programmer , Real World…

    Merck (North Wales, PA)
    …currently available through commercial software packages. + Expertise in statistics, clinical and data management concepts as applied to drug/vaccine development ... within the pharmaceutical industry; + A project leader; completes tasks independently at a project level, determines approach and ensures consistency, manages timelines; ability to communicate clearly to key stakeholders + Ability to extend existing or develop… more
    Merck (11/20/25)
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  • Biostatistical Analyst II (Remote Capable)

    Geisinger (Danville, PA)
    …+ Possesses the critical thinking skills needed to provide statistical support to clinical investigators. + Experienced SAS or R programmer for both data ... master's-level biostatistician. Responsibilities include collaborating on the design of clinical research studies, writing biostatistical analysis plans for research… more
    Geisinger (10/03/25)
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  • Sr Manager Statistical Programming

    Teva Pharmaceuticals (West Chester, PA)
    …Required: Bachelors + 7 year, Masters + 6 years in a pharmaceutical or clinical research setting as a programmer . Experience Preferred: Specialized or Technical ... for managing the timely and accurate execution of programming components of clinical trials and supports the development, regulatory approval and market acceptance… more
    Teva Pharmaceuticals (10/09/25)
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