A company is looking for an Associate Director, Statistical Programming.
Key Responsibilities
Provide technical and operational leadership for statistical programming in clinical studies and regulatory submissions
Collaborate with Biostatistics and Data Management on the development and validation of statistical datasets and specifications
Manage internal and vendor statistical programming support while ensuring quality and timely delivery across projects
Required Qualifications
At least 10 years of SAS programming experience in the pharmaceutical, biotech, or CRO industry
Experience managing programming teams and leading efforts for clinical trial reporting and submissions
Proficiency in SAS programming, including SAS / Base, SAS / Macro, SAS / STAT, SAS / Graph, and SAS / SQL
Demonstrated experience with CDISC standards, including SDTM and ADaM
Bachelor's Degree required; Master's Degree preferred in computer science, statistics, mathematics, or information sciences
Director Statistical Programming • Park Row, Texas, United States