Director, Statistical Programming
Core
Strategic leadership of statistical programming for Phase 1/2 oncology clinical trials, managing teams to deliver high-quality data products for drug development.
Role type
Director, Statistical Programming (Line Management)
Builds
Clinical trial data deliverables (statistical programming outputs) for oncology drug development programs.
Domain
Pharmaceutical clinical development / Oncology / Biometrics
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming, clinical trial principles, CDISC standards, 21CFR Part 11 compliance, regulatory submission management, team leadership, project management, resource allocation, process improvement.
Preferred skills
Oncology therapeutic area experience (heme/solid tumor), open source/AI in statistical programming, business process design.
Technologies
SAS, CDISC, 21CFR Part 11
Responsibilities
Manage and mentor a group of programmers for efficient delivery of outsourced and internal studies; ensure compliance with AZ and industry standards; provide strategic SME contributions to cross-functional teams; lead process improvements and automation initiatives.
Seniority
Director, hands-on line management & strategy
