Associate Director of Statistical Programming

A company is looking for an Associate Director, Statistical Programming.

Key Responsibilities

Lead clinical studies and provide training to team members

Contribute to and implement statistical analysis plans, and review related documentation

Create CDISC SDTM and ADaM files and perform data analysis using SAS

Required Qualifications

Minimum 10 years of programming experience in the Pharmaceutical / Biotech industry, with 2 years in a management role

Experience with FDA submissions and solid knowledge of CDISC standards (SDTM & ADaM)

Strong SAS programming skills, including SAS Base, SAS / Macros, SAS / Graph, and SAS / Stat

BS / MS or equivalent in Statistics, Math, or a related scientific discipline

Familiarity with additional software such as SpotFire or R Shiny is a plus