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    Job · 12574718

    REMOTEFULLTIME

    Statistical Programmer I, II & Senior Statistical Programmer

    Veeda Clinical Research logo

    Veeda Clinical Research

    Remote · remote · Posted 62d ago

    Sourced fromNaukri
    Undisclosed4–9 yrsfulltimeRemote

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    Section · 01

    About this role

    Position Summary:


    The Statistical Programmer I/II/Senior Statistical Programmer is responsible for building programs to create SAS datasets and working closely with other Data Management and Statistics Department staff to provide clinical programming expertise and support to clinical studies across multiple therapeutics areas, as part of the Company's global Phase I-III program.


    Role & responsibilities:


    • Writes, maintains and validates SAS programs to create templates and macros for data cleaning and reporting
    • Develops SAS programs to create and validate SDTM and performs QC of SDTM, under supervision
    • Writes SAS programs, under senior supervision, to develop ADaM datasets and ADaM TFL in accordance with CDISC standards and implementation guides
    • Programs edit checks as per given specifications
    • Performs data transfers to external recipients
    • Works closely with other Data Management and Statistics Department employees and other stakeholders to ensure accurate and high-quality deliverables
    • Complies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection

    Key competencies:


    Required-

    • Excellent knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
    • Knowledge of CDISC requirements
    • Excellent knowledge of statistical programming
    • Expertise in manipulating and analyzing SAS data

    Desired-

    • SAS Certified Programmer
    • Excellent analytical and computer skills
    • Strong communication skills
    • Ability to work in a collaborative environment
    • A genuine interest in the field of clinical development
    • Strong organizational, problem-solving, and decision-making skills
    • Ability to work according to specific SOPs, guidelines, regulations & ethical principles in

    the daily practice


    Professional Experience Requirements:


    • At least 4 to 6 years of SAS programming experience in CDISC/clinical studies in a CRO, pharma or equivalent institution

    Education Requirements:


    Required: BSc in Statistics, Mathematics, Biostatistics, Data Analysis, Data Science, or related field


    Desirable: MSc in Statistics, Mathematics, Biostatistics, Data Analysis, Data Science, or related field



    Sourced from naukri

    Section · 02

    Skills

    adamSAS ProgrammingSdtmCdisc

    Section · Company

    About Veeda Clinical Research

    Veeda Clinical Research logo

    Veeda Clinical Research

    Clinical Research

    777

    employees

    2004

    22 years old

    Ahmedabad, Gujarat

    India

    ₹4.7L PA avg

    Avg at Veeda Clinical Research

    About

    Veeda Clinical Research Limited provides end-to-end drug development services to its global clients specializing in Pharmaceuticals, biopharmaceuticals, agrochemicals, and Medical Devices.

    Industries

    Clinical ResearchPharma

    Employee ratings

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    3.5/ 5

    Culture

    2.2

    Career growth

    2.5

    Work-life

    2.7

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    Overall Company35Work-Life Balance34

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