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Clinical SAS Programmer
Clinical SAS ProgrammerKatalyst HealthCares & Life Sciences • Irving, TX
Clinical SAS Programmer

Clinical SAS Programmer

Katalyst HealthCares & Life Sciences • Irving, TX
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Responsibilities :

  • Demonstrating proficiency in CDISC, SDTM, and ADaM to support various submission activities, including IA, CSR, DSUR, and publications.
  • Providing statistical programming support to generate tables, listings, and figures for assigned projects.
  • Overseeing all aspects of statistical programming, working closely with statisticians to ensure timely and accurate delivery of statistical outputs.
  • Creating detailed specifications for individual studies and comprehensive summaries.
  • Directing and supervising CRO activities related to statistical programming, including the creation and validation of SDTM and ADaM datasets.
  • Producing safety tables, efficacy tables, and lab shift tables in accordance with the SAP and mock layouts.
  • Validating datasets and tables through double programming.
  • Having a good understanding of oncology-specific domains is an advantage.
  • Reviewing statistical analysis plans, annotated CRFs, and integrated summaries, providing thoughtful feedback.

Requirements :

  • A master's or bachelor's degree (or equivalent qualification) in a relevant field.
  • At least + years of solid experience in statistical programming with clinical trial data, particularly using SAS software.
  • A strong team player who is open to learning and adopting new methods and technologies, contributing positively to team dynamics.
  • A quick learner with a proven history of effective collaboration and teamwork.
  • Exceptional communication skills, both written and verbal.
  • Demonstrated ability to multitask, prioritize, anticipate potential challenges, and achieve goals within a multidisciplinary team environment.
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    Programmer • Irving, TX

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