About this role

Provides leadership and expertise in driving the development and maintenance of statistical programming capabilities
Manages a team of programmers supporting clinical trial and integrated analyses
Works closely with Statisticians to ensure deliverables are accurate and aligned with standards
Oversees CRO delivery or manages in-house programming of data sets, outputs, and DDT files of clinical trials
Coordinates oversight or in-house programming of exploratory analyses, secondary publications, and regulatory requests
Manages, hires, and mentors direct reports including annual evaluations and goal setting
Creates and maintains compliance with programming processes and strategy

BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
At least 10 years of experience in the biotech, pharma, or CRO industries
Preferred 5 or more years of direct supervisory experience
Experience with CRO management and/or CRO work experience
Extensive understanding of clinical programming and/or statistical programming processes and standards
Advanced Experiences with statistical programming using the SAS software including development and use of SAS Macros
Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)
Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines
Experience in working in cross-functional, multicultural and international clinical trial teams

Director, Statistical Programming

Key skills