Principal Statistical Programmer

Key Duties and Responsibilities:

• Works regularly with advanced features of SAS, including interfacing with other software applications and operating system tools.
• Performs quality control checks of SAS code and output to ensure accuracy and consistency.
• Creates all files, documents, and analyses necessary to support an electronic submission in eCTD format, including ISS/ISE.

Knowledge and Skills:

• Proficiency in all SAS language, procedures, and functions commonly used in clinical trial reporting.
• Intermediate knowledge of CDISC Standards and clinical trials.
• Effective communication skills to explain difficult information.

Education and Experience:

• Bachelor's degree in a Scientific Discipline.
• Typically requires 5+ years for M.S. or above and 8+ years for B.S. in Biotech, Pharmaceuticals, or Clinical Research Organization.