Position Details
About this role
Provide statistical programming support for multiple clinical projects across therapeutic areas, both directly and through staff. Lead standards for output design and programming conventions, guide CRF/database and derived data set/submission deliverables, and manage training and performance for a team of statistical programmers.
Key Responsibilities
- Drive SAS programming execution for non-routine problems
- Oversee global standards for output design and programming conventions
- Provide strategic guidance on CRFs and database design
- Develop/oversee derived data set specifications and submission programs
- Train, mentor, and performance-manage statistical programmers
Technical Overview
Leads SAS Programming for pharmaceutical clinical development, including global standards and specifications for CRF and database definitions, derivation programming, and submission data sets/programs. Interprets statistical analysis plans and ensures risk assessment communication and regulatory-aligned deliverable quality.
Ideal Candidate
The ideal candidate is an Associate Director-level statistical programming leader with 10+ years (MS) or 12+ years (BS) of pharmaceutical SAS programming experience. They will demonstrate deep expertise in global standards for output design, CRF/database definitions, derivation programming, and submission data set/program specifications, along with strong staff training and performance management experience.
Must-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Must have a Degree in Statistics, Computer Science, or a related field, Must meet the stated SAS statistical programming experience requirement (10+ years with MS OR 12+ years with BS), Must have strong technical competence in SAS pro, Must have staff management, training, and performance management experience
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