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  • Posted: Jun 14, 2023
    Deadline: Not specified
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  • PAREXEL has proven to be a trusted partner for the complex development journey required of biopharmaceutical and medical device companies. We’re also an astute guide, able to simplify that journey for our clients, so safe new products can reach patients more quickly. - See more at: https://www.parexel.com/company#sthash.G0bQx8Mi.dpuf


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    Clinical Data Engineer I, South Africa

    About the job:

    • The Clinical Data Engineer 1 works with close supervision to support various activities related to electronic data, and/or the application of computer and communication technologies. General areas of responsibility also include: Aggregating applicable data from all sources and devices, managing external data, programming offline listings, trend analysis, data review, data transfers.

    What You'll Do At Parexel:

    Manage Projects &Technology

    • Programming and setup of Import procedures to allow the ingestion of data either using SAS or alternative technology (e.g. “Workbench”)
    • Programming of reconciliation checks to ensure appropriate transfer of data.
    • Programming of offline listings and custom reports to allow better insights to all external data.
    • Aggrege data across all sources.
    • Handling Missing Values, reading raw data files, creating data structures, handling programming errors, accessing, and managing data, appending and concatenating SAS datasets.

    Documentation

    • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines/Work Instructions to ensure traceability and regulatory compliance. This includes the documentation of any deviations and dissemination of these to the rest of the project teams

    Ideal candidate will possess:

    • University degree in a relevant discipline.
    • Fluent English
    • Basic experience in at least one of the following (e.g. SQL, SAS, R).
    • Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICHGCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
    • Experience in clinical research industry or similar field is required.

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified? Go to PAREXEL on jobs.parexel.com to apply

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