The Principal Statistical Data Scientist will ensure the quality and timely delivery of statistical programming deliverables in pharmaceutical and biotech settings, focusing on CDISC standards. Responsibilities include programming datasets, validation checks, and ensuring adherence to software development lifecycle practices.
- 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 wor king 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 a re 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, see king direction when appropriate
- Works with statistician s 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
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.
Medical
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