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  • Posted: Nov 9, 2020
    Deadline: Not specified
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    Synteract is an innovative CRO providing full-service, Phase I-IV services to biopharma companies in bringing new medicines to market. We align our operational excellence, therapeutic expertise and the right technology to support each clients clinical development needs. Over its nearly 30-year history, Synteracts leadership has been proven in the core dev...
    Read more about this company


    DM SAS Programmer

    Position Overview

    • The SAS Programmer is responsible for executing programming activities in coordination with project teams with supervision. S/he will develop, create, verify/validate and maintain managing the programs for assigned projects in compliance with standard operating procedures.

    Specific Tasks Would Include

    • Participates in the validation of SAS programs and maintaining validation documentation.
    • Familiarizes oneself with the SAS dataset structure and format catalog related to a given study.
    • Familiarizes oneself with the documents associated with a given study.Such documents include (but are not limited to) edit check documents, SAS and database annotated Case Report Forms (CRFs), visit map/schedule of events, CRFs, code lists, statistical analysis plan (SAP), data management plan (DMP), clinical protocol, programming-specific documentation.
    • Develops, programs and maintains:
      • SAS edit checks and SAS edit check listings.
      • Subject profile programming used for quality control of paper-based project databases.
      • Data line listings as requested by the Sponsor and/or internal project teams.
      • Clean subject programming used to identify clean subjects for a given project.
      • JReview objects and registry of SAS datasets.
      • SAS programs used to generate random samples of subject numbers and calculate database reliability rate during the quality control of paper-based project databases.
      • Study Data Tabulation Model (SDTM) dataset programming.
      • Programs that download external data received from various data sources.
      • External data reconciliation programs.
      • Programs that generate CRF and Query metrics.
      • Ad-hoc Sponsor and internal programming requests.


    • Bachelor’s degree in a relevant field of study and 0-2 years data management or SAS programming experience or equivalent combination of education and experience.
    • Possess an underlying understanding of data management practices and clinical data management systems (CDMS).
    • Possess a basic understanding of the Clinical Data Interchange Standards Consortium (CDISC) domain and item names and the role of CDISC in drug development.
    • Understands the sequence of running programs to ensure up-to-date data and to troubleshoot, debug programming problems and to identify data trends.
    • Proficiency in Microsoft Office; Word, Excel, PowerPoint, Outlook as required.
    • Effective verbal and writing skills; English + local language, if relevant.

    Method of Application

    Interested and qualified? Go to Synteract on to apply

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