Related skills
r sas cdisc sdtm adam📋 Description
- Lead statistical programming for multiple trials; ensure timely, quality deliverables.
- Lead/coordinate internal/external programmers; write specs for outputs.
- Develop SAS/R programs and SDTM/ADaM specs; validate results.
- Manage computing environment, folders, access control; audit readiness.
- Collaborate with biostatistics, data management, CROs to deliver analyses.
- Oversee CROs/contractors; ensure compliance, quality, timelines, budgeting.
🎯 Requirements
- BS/MS in life sciences, CS, stats, math; 10+ years in programming/stats.
- 3+ years line management or leadership; oversee multiple trials.
- Deep knowledge of clinical trials, regulatory, and GCP.
- Advanced SAS programming: BASE SAS, SAS/STAT, SAS/GRAPH; macros; QA.
- Regulatory/CDISC knowledge (FDA/EMA/ICH); SDTM/ADaM; NDA submission exp.
- Strong interpersonal skills; ability to collaborate globally and lead teams.
🎁 Benefits
- Remote work options with US-based teams.
- Mentorship and leadership opportunities for programming staff.
- Collaborative, cross-functional environment with clinical development teams.
- Competitive benefits package.
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