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  • Posted: Sep 11, 2024
    Deadline: Not specified
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    Sharing a Vision to Drive Healthcare Forward Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources. We are inspired by the potential ...
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    Senior Statistical Programmer - Bloemfontein

    Job Overview:

    • Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.

    Program and plan the integration of databases from multiple studies or sources.

    • Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.
    • Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.
    • Fulfil project responsibilities at the level of statistical team lead for single complex studies or group of studies.

    Requirements: 

    • Bachelors or Masters’ in Computer Science, Mathematics or equivalent
    • 5+ years Statistical Programming experience within the Life-Science industry 
    • Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
    • Excellent knowledge of CDISC standards (SDTM and ADaM)
    • Excellent application development skills
    • Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
    • Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
    • In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice
    • (GCP) and International Conference on Harmonization (ICH) guidelines

    Join IQVIA to see where your skills can take you

    • Global exposure 
    • Variety of therapeutic areas
    • Collaborative and supportive team environment 
    • Access to cutting-edge and innovative, in-house technology
    • Excellent career development and progression opportunities 
    • Work-Life Balance, with a strong focus on a positive well-being
       

    Method of Application

    Interested and qualified? Go to IQVIA on jobs.iqvia.com to apply

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