**Job Description**

**Associate Principal Scientist, Statistical Programming – Rahway, NJ:**

+ Lead statistical programming activities for multiple and/or complex late-stage clinical trial development programs.
+ Develop and execute statistical analysis and reporting deliverables (e.g., safety and efficacy analysis datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.
+ Act as a key collaborator with biostatisticians, project leads, data managers, and other stakeholders in ensuring that project plans are executed efficiently with timely and high-quality deliverables.
+ Serve as the statistical programming point of contact and knowledge holder through the entire product lifecycle.
+ Develop SAS and R programs to create and validate analysis datasets (ADaM) and summaries (TFLs) in support of clinical study reports and regulatory submissions (F...