Senior Manager, Statistical Programming

Immunome seeks a Senior Manager of Statistical Programming to lead SAS programming deliverables for clinical trials, ensuring CDISC-compliant data packages and submission readiness. The role involves directing 1–2 studies through their lifecycle and collaborating across biometrics functions to enhance programming standards and infrastructure. Responsibilities Lead statistical programming for 1–2 assigned clinical studies throughout their lifecycle Develop and review programming specifications aligned with Statistical Analysis Plans Oversee creation, validation, and delivery of CDISC-compliant datasets and regulatory documentation Provide hands-on SAS programming for analyses, ad hoc requests, and regulatory submissions Collaborate on development and improvement of department programming standards and processes Requirements Extensive SAS programming experience in clinical trial environments Demonstrated expertise with CDISC standards (SDTM, ADaM, Define.xml) Experience leading statistical programming teams or managing complex study deliverables Strong knowledge of regulatory guidance and FDA submission requirements Cross-functional collaboration skills with biostatistics, data management, and clinical teams #J-18808-Ljbffr Immunome, Inc.