Associate Director, Statistical Programming

Role: Associate Director of Statistical Programming supporting clinical trial analyses within Corcept's biopharma portfolio, focusing on hypercortisolism, oncology, ALS, and liver disease. Responsibilities: lead SAS programming for statistical analyses, review and validate CRO outputs, develop CDISC-compliant data packages, and enhance programming infrastructure; collaborate with data management and biometrics teams, ensure submission readiness, and adhere to regulatory standards. Requirements: MS in Science, Statistics, or related field; 10+ years in clinical trial programming, with expertise in SAS BASE, MACRO, STAT, GRAPH, and CDISC SDTM/ADaM standards; experience with Pinnacle 21, regulatory submissions, and therapeutic areas like oncology or endocrinology preferred. High-Value: extensive SAS and CDISC knowledge, late-stage clinical development, regulatory submission experience, and management of CRO deliverables. WorkSetup: primarily on-site in Redwood City with a focus on quality and compliance.