Biostatistician II

The Biostatistician II will provide statistical support for all phases of clinical development. Responsibilities include reviewing statistical sections of protocols, writing statistical analysis plans, and developing SAS programs for tables, listings, figures and analysis datasets in accordance with Precision and/or sponsor procedures or study-specific guidelines. Essential functions of the job include generating randomization schedules, assisting with statistical methods review, providing sample size calculations, developing case report forms, and authoring statistical analysis plans. You will also generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS and assisting with quality control for statistical based SAS programs. Other tasks include providing programming and statistical support to supplemental or exploratory analyses, assisting with statistical consulting tasks, and reviewing statistical sections of clinical study reports. The role involves direct interaction with sponsors, project managers, and external vendors on statistics-related project components, completion of statistical activities within timelines, providing units for development of monthly project invoices, and training/mentoring new biostatisticians.