Principal Statistical Programmer
Location: Bangalore, India
Job Type: Full-Time
Application Deadline: January 26, 2026
Experience Required: 10–11+ years in statistical programming/clinical data analysis
Job ID: R1508100
Company Overview
IQVIA is a global leader in clinical research, healthcare intelligence, and life sciences solutions. We accelerate the development and commercialization of innovative medical treatments by leveraging advanced analytics, technology, and domain expertise. Our teams deliver high-quality solutions that improve patient outcomes while supporting pharmaceutical and biotech clients globally.
Role Overview
The Principal Statistical Programmer is a senior-level role providing advanced technical expertise and leadership for complex clinical trials. This role ensures the design, development, and integration of statistical programming solutions across studies, maintaining high standards of data quality, regulatory compliance, and operational efficiency. The Principal Programmer also mentors junior staff and contributes to strategic process improvement initiatives.
Key Responsibilities
Lead statistical programming for complex studies, including:
Programming, testing, and documenting programs for tables, listings, and figures.
Developing analysis datasets (derived datasets) and managing data transfers.
Conducting database quality control checks and ensuring integration across multiple studies.
Plan, implement, and validate new programming technologies, macros, and applications.
Coordinate and maintain detailed programming documentation, specifications, and plans.
Provide technical expertise and independent solutions for complex client requirements.
Fulfill project responsibilities at the level of statistical team lead for single or multiple studies.
Manage project budgets, scope, resource forecasts, and revenue estimates.
Mentor, train, and guide junior statistical programmers to enhance departmental capabilities.
Qualifications & Experience
Education:
Master’s degree in Computer Science or related field with 10 years relevant experience, or
Bachelor’s degree in Computer Science or related field with 11 years relevant experience, or
Equivalent combination of education, training, and experience.
Technical Skills:
Advanced expertise in Base SAS, SAS Graph, and SAS Macro Language.
Strong knowledge of statistics and clinical drug development processes.
Professional Skills:
Excellent leadership, organizational, interpersonal, and communication skills.
Proven ability to manage multiple complex tasks and projects.
Strong attention to detail and accuracy.
Ability to establish and maintain effective working relationships with clients, managers, and colleagues.
Why Join IQVIA
Lead statistical programming for high-impact global clinical trials.
Collaborate with cross-functional teams in a world-class CRO environment.
Mentor junior programmers and shape programming processes for departmental efficiency.
Competitive compensation and opportunities for career growth in a global organization.
Apply Now via thepharmadaily.com to join IQVIA as a Principal Statistical Programmer and drive innovative clinical research solutions globally.
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