Sr. Principal Analyst, Statistical Programming
Neurocrine Biosciences · San Diego
BiometricsFull-time$157k–$214kCompany career page
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What they're looking for
- Bachelor's degree in computer science, mathematics, statistics, or related field plus 8+ years biopharmaceutical statistical programming experience
- Master's degree in relevant discipline plus 6+ years similar biopharmaceutical statistical programming experience
- PhD in relevant discipline plus 4+ years similar biopharmaceutical statistical programming experience
- Advanced SAS proficiency (Base, Stat, Macro, Graph) and CDISC data structures expertise
- Minimum 2 years supervisory or lead programming experience
- Expert knowledge of SDTM domains, ADaM datasets, Define.xml, and regulatory standards (ICH, 21 CFR Part 11, FDA guidelines)
- Demonstrated proficiency managing large projects, external vendors, and multi-disciplinary cross-functional teams
What you'll be doing
- Lead statistical programming work-streams across multiple clinical programs and multidisciplinary teams
- Mentor and manage statistical programmer team supporting clinical and nonclinical data analysis and reporting
- Develop SAS programs for clinical data evaluation and establish programming standards, conventions, and infrastructure
- Direct vendor selection, validation of programming activities, and e-submission requirements for regulatory deliverables
- Provide workforce planning recommendations and serve as lead or quality control programmer on assigned projects
Privacy & handoff
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