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    Principle Statistical Programmer - Philadelphia, United States - Saxon Global

    Saxon Global
    Saxon Global Philadelphia, United States

    2 weeks ago

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    Description

    Role- Senior Clinical SAS Programmer

    Rate-$65-70/hr On C2C

    Work Auth-All Except H1B

    Long-term CONTRACT years)

    REMOTE POSITION

    JOB DESCRIPTION

    A leading global biopharmaceutical company is looking for multiple Sr. Statistical/Lead/Principle Statistical Programmer responsible for processing clinical data required for statistical analysis of Phase I - III clinical trials, and leading project teams. We would like to fill this position as soon as possible years statistical programming experience with pharmaceutical/ CRO industry is required. Strong Macro Development experience is required. PK/PD Programming is a big plus.

    Key Responsibilities

    • Provide quality deliverables by following corporate and departmental policies, procedures and applicable standards
    • Perform data manipulation, analysis and reporting of clinical trial data
    • Create analysis files, tables, listings, and figures and validation of those files
    • Maintain project tracking and validation documentation
    • Work well in an environment where team members may be distributed across multiple locations
    • Review planning documents (Statistical Analysis Plan, dataset specifications, etc.) to ensure project objective alignment, clarity, accuracy and completeness of programming requirements
    • Present statistical programming concepts to non-programming team members as necessary
    • Collaborate effectively with cross-functional teams and interface with multiple stakeholders to manage timelines and priorities
    • Serve as back-up to Principle Statistical Programmer as needed
    Required Qualifications
    • BA/BSc or Master's in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject with 7-8+ years of relevant experience
    • Extensive regulatory submission and response experience
    • In depth SAS Programming background with excellent analysis and reporting skills
    • Command of drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
    • Thorough knowledge of latest CDISC SDTM, ADaM and Define standards
    • Ability to effectively oversee geographically diverse programming teams
    • Familiarity with other programming languages (e.g. Java, R, or S-Plus)
    • Project management or project planning experience on small to large scale drug development projects
    • In depth knowledge of SAS Graph and Stat packages
    Search Terms: Statistical Programmer, Clinical SAS Programmer, Senior Statistical Programmer, Lead Statistical Programmer, SAS Programmer, Clinical SAS Programmer, SAS Analyst, statistical programming, clinical data,SAS Software, CDISC, SAP, CDISC validation, OpenCDISC, ADaM datasets, CDISC compliant, SAS macros, Statistical Analysis Plan, clinical trials, SAS Base/Stat/Macro/GRAPH, MS in statistics. MS in Mathematics, Statistics, Biostatistics
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