Senior Statistical Programmer
ROLE OVERVIEW
Based at AstraZeneca's Manyata Tech Park campus in Bangalore, the Senior Statistical Programmer I role sits within the Oncology Biometrics Programming department—a critical function that turns raw clinical trial data into regulatory-ready evidence. As part of a global team dedicated to eliminating cancer as a cause of death, you will support and lead statistical programming activities across high-priority oncology studies, from clinical study report development to regulatory submissions and commercialisation. This is a compelling opportunity for an experienced SAS programmer who wants to see their code influence filings, accelerate patient access, and shape evidence-based decisions. AstraZeneca's deep pipeline, collaborative research culture, and investment in science and technology make this a career-defining platform for professionals who combine technical rigour with a passion for improving patient outcomes.
ROLE DEFINITION & RESPONSIBILITIES
- •Develop, validate, and maintain SAS programs for analysis datasets, tables, listings, and figures (TLFs) in accordance with study protocols and statistical analysis plans.
- •Lead statistical programming activities at study or project level, ensuring timely delivery of analysis and reporting outputs for oncology clinical trials.
- •Implement CDISC standards, including SDTM and ADaM, to create submission-ready datasets for regulatory filings.
- •Collaborate with biostatisticians, data managers, clinical scientists, and medical writers to interpret data and resolve programming issues.
- •Perform quality control reviews, double-programming, and validation of deliverables to ensure accuracy and regulatory compliance.
- •Support regulatory submissions, responses to health authority questions, and commercialisation activities by providing programming expertise.
- •Mentor junior programmers, manage stakeholder expectations, and contribute to process improvement initiatives within Biometrics Programming.
- •Maintain detailed documentation of programming activities and ensure audit-ready traceability throughout the study lifecycle.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's or Master's degree in Mathematics, Statistics, Computer Science, Life Sciences, or a related discipline.
- At least 3 years of industry statistical programming experience with a Master's degree, or 5+ years with a Bachelor's degree.
- Extensive hands-on SAS programming expertise at an advanced level within clinical drug development.
- Comprehensive knowledge of technical and regulatory requirements for pharmaceutical programming.
- Good knowledge of CDISC standards (SDTM, ADaM) and industry best practices.
- Proven ability to lead studies or programming activities within clinical trials.
- Excellent verbal and written communication skills, with the ability to influence and collaborate in a global team.
PREFERRED QUALIFICATIONS
- •Oncology TA experience
- •Submission experience
- •Lead experience
- •Spotfire or R programming
- •Mentoring junior programmers
REQUIRED VERIFIED SKILLS
COMPENSATION & REWARDS
ORGANIZATION CONTEXT & CULTURE
AstraZeneca is a global, science-led biopharmaceutical company focused on the discovery, development, and commercialisation of prescription medicines. The company operates in various therapeutic areas, including Oncology, Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. AstraZeneca is committed to pushing the boundaries of science to deliver life-changing medicines and improve patient outcomes worldwide.
EXPECTED CAREER ROADMAP
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