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.