Senior Statistical Programmer

Responsibilities:

• Develop or review and QC CDISC-compliant datasets (SDTM & ADaM) and corresponding documentation for electronic submission.
• Develop SAS programs to generate or QC displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies, internal deliverables, and publications.
• Ability to write new SAS macros or incorporate existing SAS macros into individual programs.
• Review and provide input on key study-related documents (e.g., CRFs, SAPs, etc.).
• Review and remain compliant with SOPs and Technical Guide documents related to Statistical Programming.
• Review and update documentation for tracking programming assignments and progress.
• Other tasks related to statistical programming efforts as required.

• 7+ years of statistical programming experience in life sciences.

• Recently experience working in a small team/small company environment (Sponsor).
• Skilled SAS programming expertise and the ability to program CDISC datasets from scratch (SDTM & ADaM).
• Ability to jump into a complex study and get up to speed quickly with little to no training time.