Senior Statistical Programmer I

Role Overview AstraZeneca is looking for a Senior Statistical Programmer to join its Oncology Biometrics Programming department at Manyata Tech Park, Bangalore. This is a hybrid role where you will provide expert statistical programming support and lead activities related to clinical data analysis and reporting across multiple studies. Your work will directly contribute to drug development, regulatory submissions, and life-changing oncology medicines. Key Responsibilities - Deliver statistical programming support for clinical study reports, regulatory submissions, and commercialisation activities - Lead or contribute to analysis and reporting processes at the project and study level - Develop and validate SAS programs in compliance with CDISC standards and regulatory requirements - Collaborate with global biometrics teams and cross-functional stakeholders to ensure accurate and timely delivery - Apply advanced SAS programming expertise to manage concurrent studies and programming tasks independently - Support scientific utilisation of clinical data for AstraZeneca oncology products Required Qualifications - Bachelor's or Master's degree in Mathematics, Statistics, Computer Science, Life Sciences, Social Sciences, or a related field - Minimum 5 years of industry experience with a Bachelor's degree or at least 3 years with a Master's degree - Advanced SAS programming skills within a clinical drug development environment - Strong knowledge of CDISC standards and pharmaceutical industry best practices - Prior experience leading studies or activities within clinical trials - Excellent verbal and written communication skills with the ability to influence team members - Ability to multitask, work independently, and manage competing priorities with attention to detail Why Join Us At AstraZeneca, you will be part of a purpose-driven team that combines bold science, technology, and human ingenuity to defeat cancer. This is your opportunity to see your programming work featured in high-impact regulatory filings and studies while building a rewarding career in one of the world's leading pharmaceutical companies.

- Advanced SAS programming expertise in clinical drug development - Knowledge of CDISC standards and regulatory requirements - Bachelor's or Master's in Mathematics, Statistics, Computer Science, Life or Social Sciences - 5+ years of industry experience (Bachelor's) or 3+ years (Master's) - Experience leading clinical trial studies or programming activities - Strong attention to detail and ability to handle concurrent projects - Excellent verbal and written communication skills - Ability to work independently and as part of a global team

- Hybrid work model with flexible in-office arrangements - Opportunity to work on high-impact oncology drug development programmes - Diverse and inclusive workplace culture - Career development and progression opportunities within a global pharmaceutical leader - Collaborative research environment connecting academia and industry