Clinical SAS Programmer

4 weeks ago

Basking Ridge, United States Katalyst Healthcares and Life Sciences Full time
Responsibilities
  • Define and edit mock tables, listings and figures (TLFs) and analysis dataset specifications.
  • Generate, document, and maintain analysis datasets.
  • Develop scripts for wrangling / data transformation and standardizing assay datasets.
  • Create ad hoc, standard and study-specific reports (e.g. SMC, DSMB, SMB, Assay QC); may perform cross-study reporting.
  • Test and de-bug programs and maintain version control on production programs and scripts.
  • Design and develop new work instructions (WIs) and updates to existing WIs.
  • Work with clinical programmers, lab programmers, statisticians, and other statistical programmers to resolve data quality, processing, and analysis issues.
  • Contribute to mentoring and training of junior Statistical Programmers and may supervise as neede
Requirements:
  • Bachelor's degree in computer science or a scientific, technical, or health-related field.
  • t least five years of experience in R programming, with additional experience in other programming languages, experience using version control tools (e.g. git or svn).
  • t least four years of experience in support of clinical trials, in clinical research setting or other health research setting, or in data wrangling/transformation within a health-related field.
  • Demonstrated ability to communicate effectively in a matrix management environment as a member of several project teams.
  • Knowledge of and experience with clinical trials research data.
  • Graduate degree in computer science or a scientific, technical, or health-related field.
  • 3+years of statistical programming in clinical research setting or R programming in a health-related field.

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