Clinical SAS Programmer - Katalyst Healthcares & Life Sciences

• Process Electronic Data Capture (EDC) data into analytical datasets
• Create Tables, Listings, and Figures to support Regulatory Clinical Trials
• 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:

• BS in Statistics, Computer Science, Mathematics, or a similar field. Work experience will be considered.
• Deep knowledge of SAS. Skills in R and Python are a plus.
• Programming experience in the CRO or Pharmaceutical industry
• Knowledge of data standards for clinical research and statistical analysis (e.g., CDISC, SDTM, ADaM, ICH Statistical Principles for Clinical Trials)
• Excellent oral and written communication skills
• Ability to read, analyze, and interpret complex documents.
• Strong organization skills and flexibility to respond to changing deadlines.