Director, Statistical Programming
Core
Lead statistical programming for Phase 1/2 oncology clinical trials, managing a team of programmers to deliver high-quality data products for regulatory submissions.
Role type
Senior IC statistical programming director (line management)
Builds
Clinical study data sets and regulatory submission packages for oncology trials
Domain
Pharmaceutical clinical development (Oncology)
Required skills
SAS programming, clinical trial principles, CDISC standards, 21CFR Part 11, regulatory submissions, team leadership, project management, process improvement
Preferred skills
Oncology therapeutic area experience, cross-functional collaboration, strategic planning
Technologies
SAS
Responsibilities
Manage and mentor a group of programmers; ensure compliance with AZ and industry standards (GxP, SOPs); provide strategic SME contributions to cross-functional teams; lead process improvements and automation initiatives.
Seniority
Director, hands-on IC with line management