Lead the Statistical Programming group at Neumora to support compounds in clinical development, regulatory filing, and commercialization. Responsible for ensuring accuracy of post-EDC datasets, performing statistical data analysis, managing study timelines, and creating SOPs for statistical programming activities.

Lead biostatistician role at Neumora, providing statistical leadership for clinical trials and data analysis. Responsibilities include protocol development, study SAP creation, managing statistical vendors, and regulatory document contribution. Requires a PhD in statistics or biostatistics with at least 10 years of experience in clinical trial design and analysis.