Related skills
r ai sas cdisc sdtm📋 Description
- Support the statistical programming function by implementing SOPs for trials
- Lead programming activities for projects and submissions with high quality
- Manage CROs/external vendors for quality and compliance
- Collaborate with Biostatistics, Data Management, Clinical Ops, Regulatory, and PV
- Develop data review, reporting tools, and statistical apps with cross-functional teams
- Review SAS programs (SDTM, ADaM, and TFLs) and SAPs/CRFs
🎯 Requirements
- Master’s degree in Statistics, Biostatistics, Mathematics, Computer Science, or related field
- 12–15 years of clinical trial programming in biotech/pharma with leadership
- Advanced SAS programming; experience with R or other languages
- Strong CDISC SDTM/ADaM knowledge and controlled terminology
- Experience mentoring programmers and managing CROs; cross-functional collaboration
- AI in drug development; automation; cloud platforms; remote work
🎁 Benefits
- Culture rooted in CORE values: Caring, Original, Resilient, Egoless
- Fast-paced environment with opportunities to wear multiple hats
- Competitive compensation and equity, plus health and retirement benefits
- Paid time off: 3 weeks PTO, two shutdowns, paid sick leave
- Professional growth with development resources and learning opportunities
- Regular all-team in-person meetings to build relationships
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