Statistical Programming Portfolio Lead, Associate Director
Core
Lead statistical programming activities and information management for clinical drug development projects within the Cardiovascular Renal Metabolism (CVRM) Biometrics team.
Role type
Senior IC statistical programming portfolio lead (Associate Director)
Builds
High-quality statistical analysis deliverables, submission strategies, and automated solutions for clinical trials.
Domain
Clinical drug development / Biostatistics / Regulatory submissions
Deliverable
production ML models | product features | dashboards & analysis
Required skills
Statistical programming, clinical development process knowledge, team leadership, risk management, regulatory requirements expertise
Preferred skills
Cross-therapeutic area experience, regulatory submission interaction, business process design
Technologies
SAS, R, Python (implied by statistical programming context)
Responsibilities
Oversee delivery of data according to industry standards, plan and execute submission strategies, provide subject matter expertise in statistical programming, lead implementation of programming activities, act as a specialist in cross-functional teams
Seniority
Senior, hands-on IC with leadership responsibilities