Covance

  • Statistical Programmer 1

    Job Location(s) US-NC-Wilmington
    Job Number
    2018-26143
    Job Category
    Biostatistics/Programming
    Position Type
    Intern
  • Job Overview

    Statistical Programmer 1

    Temporary, Part-Time

     

    • Provide Statistical Programming service
    • Develop and review SAS programs and output for the management and reporting of clinical trial data including ADaM and client-defined analysis datasets, tables, listings and graphs.
    • Develop programs for data transfers and assist in their review to ensure the data transfer has been produced to specification
    • Review draft and final production runs for project to ensure quality and consistency.
    • Ensure quality of personal work
    • Interact with project team members in related discipline e.g. Clinical Data Management., Clinical Operations and Biostatistics.
    • Prioritize personal workload to meet specified completion dates
    • Display a positive attitude at all times, promoting and contributing to good team spirit in a professional environment
    • Develop good problem solving skills and a willingness to learn and seek advice from senior Statistical Programming staff
    • Acquire knowledge of other aspects of the work of a Statistical Programmer Analyst under the supervision of the senior Statistical Programming staff
    • Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
    • Perform other duties as assigned by senior Statistical Programming staff

    Education/Qualifications

    Minimum Required:

    • Attempting a BSc in a computing, life science, mathematical or statistical subject (not completed).
    • A high computing content is considered to be beneficial, however proven computing skills are most important
    • Alternative academic qualification or experience are assessed to ensure equivalent background

    Experience

    Minimum Required:

    • programming knowledge using SAS or other programming language; Knowledge of fundamental principles of programming and program development
    • Some understanding of the clinical trial process
    • Good organizational skills and the ability to prioritize own work
    • Self motivation
    • Good time management skills and the ability to work to tight deadlines whilst maintaining the highest standards of work
    • Effective communication skills
    • A cooperative and team oriented approach

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