Statistical Programming Strategy & Portfolio Lead, Associate Director
Core
Provide strategic programming leadership, planning, and project management for clinical drug development programs within the Cardiovascular Renal Metabolism (CVRM) Biometrics team.
Role type
Senior IC statistical programming strategy lead (no formal line management)
Builds
High-quality statistical analyses, reporting deliverables, and submission strategies for clinical trials
Domain
Clinical drug development / Biostatistics / Regulatory submissions
Required skills
SAS programming, CDISC standards, clinical development process knowledge, project management, risk management, team development, regulatory requirements awareness
Preferred skills
Cross-therapeutic area experience, regulatory submission experience, business process design, travel
Technologies
SAS, CDISC
Responsibilities
Oversee delivery of data according to industry standards, plan and execute submission strategies, drive continuous improvement and automation solutions, provide subject matter expertise in statistical programming
Seniority
Associate Director, strategic leadership