Associate Director, Statistical Programming

Nuvalent is seeking an Associate Director, Statistical Programming to lead statistical analyses using SAS and perform quality review of SAS programs and deliverables. The role will work closely with Biostatistics, Data Management, Clinical Operations, and other related disciplines.

Requirements

• Master's Degree in statistics, mathematics, computer science, or related scientific/medical field
• 8+ years of (SAS) statistical programming experience in a clinical trial setting (industry/CRO)
• Advanced SAS programming skills - procedures and options commonly used in clinical trials
• Hands-on knowledge of CDISC SDTM and ADaM models and transforming raw data into these standards
• Oncology experience is required

Benefits

• Equal employment opportunities
• Comprehensive benefits package (not specified)