Senior/ Principal Statistical Programmer

📋 Description Lead end-to-end statistical programming for ADaM datasets and TLFs. Support regulatory deliverables incl. ISS, ISE, and submissions. Develop and maintain CDISC SDTM/ADaM datasets per industry standards. Create reusable utilities, macros, and automation solutions. Build analysis cohorts and work with RWD and external controls. Apply survival analysis and propensity score methods. 🎯 Requirements 6–10+ years of experience in statistical programming in clinical research. Strong hands-on R programming with 1–3+ years practical experience. Solid SAS programming with clinical trial workflows. CDISC SDTM/ADaM knowledge; experience generating datasets and deliverables. Experience with RWD/RWE, biomarker data, external controls. Familiarity with oncology/respiratory/immunology areas preferred. 🎁 Benefits Fully remote work opportunity. Long-term contract with meaningful clinical projects. Competitive salary based on experience. Work with advanced statistical programming methodologies. Exposure to global clinical development and regulatory submissions. Flexible work environment for experienced professionals.