Associate Director, Statistical Programming

📋 Description

• Lead statistical programming for multiple trials in a program.
• Ensure CDISC-compliant data handling with biostatistics.
• Audit readiness and quality of programming deliverables.
• Lead SAS programs for TLFs and analysis datasets.
• Coordinate internal/external programmers; set strategies.
• Manage timelines and CRO/contractor oversight.

🎯 Requirements

• BS/MS in life sciences, CS, statistics, or equivalent; 10+ years.
• 3+ years line management or leadership; oversee multiple trials.
• Advanced SAS in clinical trials; Base SAS, SAS/STAT, macros, TLFs.
• SDTM/ADaM experience; submission-ready deliverables.
• CDISC standards and regulatory knowledge (FDA/EMA).
• Experience outsourcing programming to CROs/vendors; timelines/budgets oversight.
• Strong communication and leadership; global collaboration.
• R, Spotfire, or Generative AI tools a plus.

🎁 Benefits

• Annual bonus and equity compensation.
• Competitive benefits package.
• Remote or onsite flexibility.
• Career growth and mentoring.
• Global, collaborative team environment.
• Culture of innovation and high standards.