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
Associate Director of Statistical Programming • San Francisco, California, United States