Senior Statistical Programmer / Statistical Programming Scientist

Role & Responsibilities
• Perform end-to-end statistical programming activities including SDTM, ADaM, and TFL development
• Support clinical studies across Oncology, Virology, and Inflammation therapeutic areas
• Ensure high-quality, compliant deliverables aligned with regulatory standards
• Collaborate with biostatistics, clinical, and data management teams
• Perform QC, validation, and documentation of statistical outputs
• Support submissions, audits, and inspection readiness activities

Qualification
• Bachelor’s or Master’s degree in Statistics, Mathematics, Life Sciences, or related discipline
• Strong knowledge of clinical trial data standards (CDISC – SDTM, ADaM)
• SAS programming expertise is mandatory

Experience
• Minimum 8+ years of end-to-end statistical programming experience
• Hands-on experience in SDTM, ADaM, and TFL development
• Prior experience in Oncology, Virology, or Inflammation studies preferred
• Exposure to regulatory submissions and global clinical trials

Skills
• Advanced SAS programming skills
• Strong understanding of clinical trial processes and GCP
• Attention to detail and strong analytical mindset
• Ability to work independently in a hybrid / virtual environment
• Effective communication and stakeholder collaboration skills

Hiring Details
• Virtual Interview Drive
• Date: Friday, January 30, 2026
• Work Model: Hybrid
• Multiple locations available

About the Company
• IQVIA is a global leader in clinical research, data analytics, and healthcare intelligence,    Works with leading pharmaceutical and biotech companies worldwide.