• At least 5 - 6 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
• Accountable for the quality and timely delivery of of enterprise, study and asset level deliverables of standard statistical programming encompassing the following areas: CDISC SDTM, ADaM, and TLF generation
• Demonstrate experience working as part of a software development team and fundamental SDLC processes
• Ensures excellence in the understanding of CDISC IG requirements, NCI Control Terminology, and programming of analysis ready datasets, tables, listings, and figures for which they are responsible
• Ensures adherence to Pinnacle 21 CDISC validation checks and high quality programming standards in their daily work
• Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate
• Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place
• Will be knowledgeable of software development practices as defined within Pfizer’s CDISC development framework
• May contribute to department level initiatives

  
Work Location Assignment: Flexible

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.