Senior Statistical Programmer for Clinical Trials

22 hours ago


Philadelphia, Pennsylvania, United States Katalyst HealthCares & Life Sciences Full time

Katalyst HealthCares & Life Sciences is seeking an experienced Clinical SAS Programmer to join our team.

About the Role

This position offers a unique opportunity to work with cutting-edge technology and contribute to the success of our clinical trials.

We are looking for a highly skilled programmer who can process Electronic Data Capture (EDC) data into analytical datasets, create Tables, Listings, and Figures to support Regulatory Clinical Trials, and develop and maintain SAS programs for data importing, quality assurance, and reporting.

Responsibilities
  • Process EDC data into analytical datasets using advanced statistical techniques.
  • Create high-quality Tables, Listings, and Figures to support regulatory submissions.
  • Develop and maintain SAS programs for data importing, quality assurance, and reporting.
  • Produce Define XML/PDFs, aCRFs, and Reviewers Guides to support SDTMs and ADaMs.
Requirements
  • A Bachelor's degree in Statistics, Computer Science, Mathematics, or a related field.
  • Deep knowledge of SAS programming language, with experience in developing complex programs.
  • Skills in R and Python are a plus.
  • Experience in the CRO or Pharmaceutical industry, with knowledge of data standards for clinical research and statistical analysis.
  • Excellent oral and written communication skills.
  • Ability to read, analyze, and interpret complex documents.
  • Strong organization skills and flexibility to respond to changing deadlines.
Salary and Benefits

We offer a competitive salary of $110,000 per year, based on experience and qualifications. Our comprehensive benefits package includes health insurance, retirement savings plan, and paid time off.



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