Associate Director of Statistical Programming

A company is looking for an Associate Director of Data Standards & Statistical Programming.

Key Responsibilities

Plan and track statistical programming activities including SAS macro development

Coordinate tasks across multiple studies and collaborate with CRO, Biostatistics, and Data Management

Oversee the workflow of clinical data listings, summary tables, figures, and Define.xml files

Required Qualifications

MS in mathematics, statistics, computer science, or equivalent

12+ years of statistical programming experience in the Bio-Pharma industry using SAS

At least 8 years of experience with CDISC SDTM and ADaM standards

A minimum of 4 years in oncology clinical trials

Solid knowledge of SAS programming language and proficiency in SAS Base, SAS / Macros, SAS / Graph, and SAS / Stat