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Clinical SAS Programmer

Company: Katalyst Healthcares & Life Sciences
Location: Bayonne
Posted on: January 16, 2023

Job Description:

Responsibilities:


  • Extract clinical data from the clinical data management system and produce standard and custom reports, primarily in SAS.
  • Program reports and listings as requested by project team members for ongoing studies. Develop transfer specifications with vendors for external data sources.
  • Perform consistency checks on data transferred between Incyte and external parties to ensure completeness and accuracy of data contained transfers.
  • Perform programming to convert raw, clinical trial data to Study Data Tabulation Model (SDTM) format.
  • Perform Quality Control (QC) on programming work performed by fellow Database Programmers.
  • Create and validate global macros or systems that streamline repetitive operations to increase programming efficiency.
  • Qualifications (Minimal acceptable level of education, work experience, and competency)

    Requirements:


    • Bachelor's degree OR certification.
    • Minimum of 2 years of clinical SAS programming experience in the pharmaceutical industry.
    • Working knowledge of CDISC SDTM mapping/specs/conversion/domains/datasets/eCRF/eCRT
    • Package/define.xml development and SDTM data transfer operations on clinical studies.
    • Understanding of regulatory requirements relevant to submissions.
    • Knowledge of clinical trial study design and electronic data submission requirements.
    • Communication and interpersonal skills and the ability to work effectively as part of a team.



Keywords: Katalyst Healthcares & Life Sciences, Bayonne , Clinical SAS Programmer, IT / Software / Systems , Bayonne, New Jersey

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