• Biostatistician II

    Job Location(s) IN-Bangalore
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  • Job Overview

    • Interaction with members of assigned project teams from other disciplines.
    • Preparation of statistical analysis plans under the supervision of senior statistical staff.
    • Assure quality of personal work.
    • Perform QC/statistical review of data displays for study endpoints.
    • Statistical analysis of clinical trial data using basic methodology, under the supervision of senior statistical staff.
    • Generate randomization schedules from provided specifications.
    • Maintain project administration files with regard to all documents produced by Biostatistics, including associated review, QC and project tracking information, and internal and external communications.
    • Maintain electronic files generated in Biostatistics according to defined specifications and procedures, ensuring those of a temporary nature are deleted in a timely fashion.
    • SAS programming and related activities for the presentation and analysis of clinical trial data.
    • Carry out all activities according to appropriate Covance SOP’s working within the framework of the quality management system and to GCP and perform other duties as requested by Management.


    MA or MSc in Statistics subject, preferably with a strong medical statistics component (alternate academic qualifications are assessed for comparability).


    3 to 5 years of post graduate experience in the application of statistics to clinical trials for the employees with an MA/MSc in statistics subject; or 0 to 3 years of postgraduate experience in the application of statistics to clinical trails for the employees with a Ph.D. in statistics subject.


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