Associate Director, Statistical Programming

Responsibilities:

• Function as lead programmer to produce and/or validate tables, listings, figures, and analysis datasets.
• Develop/review TFL shells, SDTM and ADaM specifications in collaboration with biostatisticians.
• Work closely with Data Management and Biostatistics to ensure final databases analyses.

Qualifications:

• Master’s Degree in statistics, mathematics, computer science, or related scientific/medical field.
• 8+ years of (SAS) statistical programming experience in a clinical trial setting (industry/CRO).
• Hands-on knowledge of CDISC SDTM and ADaM models and transforming raw data into these standards.

Competencies:

• Adaptability/Flexibility – The ability to adapt to working effectively within a variety of situations.
• Communication and Teamwork – Ability to effectively express ideas in written and oral context.
• Problem Solving – Ability to understand a situation or problem by breaking it down into smaller pieces.