Statistical Programming, Associate Director
Core
Lead statistical programming activities for clinical study planning, execution, and delivery, including clinical study report development and regulatory submissions for oncology products.
Role type
Senior individual contributor statistical programming lead (Associate Director)
Builds
Clinical study reports, regulatory submissions, and scientific data utilization for oncology drug development
Domain
Pharmaceutical / Clinical Trials / Oncology
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
SAS programming, CDISC standards, clinical study report development, regulatory submission knowledge, project leadership, statistical analysis
Preferred skills
None stated
Technologies
SAS
Responsibilities
Lead statistical programming activities at the project/study level, manage concurrent projects, collaborate with global teams, influence stakeholders
Seniority
Senior, hands-on IC with management responsibilities
