Jobs at Annexon Biosciences

Lead and oversee statistical programming for clinical trials and regulatory submissions. Manage vendor-delivered programming, develop and verify CDISC SDTM/ADaM datasets and submission packages, review SAP/TFL shells/eCRFs, maintain auditable documentation, perform gap analyses for global submissions (BLA/MAA), support ad hoc submission/publication requests, and provide cross-functional guidance to study teams.

The Director of Quality Systems ensures compliance and operational excellence of Annexon's Quality Management System while leading electronic quality systems and validation activities. Responsibilities include supporting audits, managing document control, and driving continuous improvement initiatives.

The role involves leading contract negotiations for various procurement agreements, partnering with internal stakeholders, optimizing vendor relationships, and refining procurement processes.