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r sas sap cdisc sdtm📋 Description
- Lead statistical programmer on multiple clinical studies
- Oversee programming vendors and activities
- Review datasets and TFLs from vendors
- Collaborate with Biostatistics, Data Management and Clinical Ops to deliver on-time data
- Develop and implement programming processes and standards
- Build and mentor a team of programmers
🎯 Requirements
- Master’s Degree in Statistics, Biostatistics, Mathematics, Epidemiology or related
- 10+ years in clinical trial programming in biotech/pharma
- Advanced SAS programming; experience with R or similar stats software
- CDISC knowledge: SDTM, ADaM and controlled terminologies
- Experience managing CROs and data vendors
- Remote-friendly; up to 15% travel; strong org/communication skills
🎁 Benefits
- Strong culture built on C.O.R.E. values
- Fast-paced environment with growth opportunities
- Competitive compensation: base salary, bonus, equity, benefits
- Generous paid time off: 3 weeks PTO, two shutdown weeks, sick leave
- Professional development resources
- Regular all-team in-person meetings
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