Principal Statistical Programmer is responsible for serving as technical lead and project manager for multiple studies, managing all aspects of study deliverables related to statistical and clinical programming. The role requires ensuring high quality, traceability, reproducibility, and timeliness of statistical programming deliverables to meet expectations and regulatory requirements.
Requirements
- Master's in Statistics, Pharmacology, Health Care, or related field
- Six years of experience as a statistical programmer conducting statistical analysis to support clinical development in the pharmaceutical industry
- Experience with Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) guidelines
- Experience with using SAS and R
- Experience with managing projects that follow Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines
Benefits
- medical
- dental
- vision
- flexible time off
- 401(k)
- life and disability insurance
- recognition programs