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    Statistical programmer - New York, United States - Katalyst HealthCares & Life Sciences

    Katalyst HealthCares & Life Sciences
    Katalyst HealthCares & Life Sciences New York, United States

    1 week ago

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    Description
    Responsibilities:
  • A statistical programmer consultant provides timely support to the study team on all programming matters according to the project strategies.
  • Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent implements and executes the programming and project standards.
  • Works independently in the design and testing of program logic, coding programs, program documentation and preparation of programs. Supports ongoing clinical studies requests for statistical and non-statistical analyses.
  • Meets statistical ad hoc requests of senior management.
  • Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.
  • Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions.
  • Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.

    • Requirements:

  • Support programmer within a study team involved in the creation and QC of analysis datasets TFL's or standard tools following Regeneron standard data models or user requirements.
  • Apply standard tools developed for the study or project. Participate in development of new standards and tools.
  • Follow all company SOP and guidelines in the creation of the programming deliverables.
  • Adheres to procedures surrounding retention of data, records, and information for clinical studies.
  • Experience and Required Skills: Requirements:
  • SAS, (Base, Stat, Macro, graph).
  • MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with - years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. SAS Certification a plus.
  • Experience in SAS programming, preferably in a clinical data environment.
  • Exposure of relational database structure
  • Understanding of reporting systems.
  • Experience with implementing standardization methodology.
  • Demonstrated teamwork and interpersonal skills, strong verbal and written communication skills in a global environment.
  • Ability to support study requirements with challenging timelines under direct supervision by the programming lead.
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