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 Pfizers CDISC development framework
May contribute to department level initiatives
Work Location Assignment: Flexible Work Location Assignment: FlexiblePfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Medical#LI-PFE