Senior Statistical Programmer II

AstraZeneca; Bengaluru; Hybrid; INR 1,200,000 - 2,100,000; Full time

Job summary

AstraZeneca is seeking a Senior Statistical Programmer II for the Oncology Biometrics Programming team at Manyata Tech Park, Bangalore. The role is hybrid, involving statistical programming support and leadership on study-level analyses for regulatory submissions and reporting in clinical development.

The candidate will contribute to SRD development, data utilization, and regulatory interactions, with opportunities for continued career growth in a science-led company that values collaboration

Qualifications

• Bachelor's or Master's (or local equivalent) in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field.
• At least 3 years of industry experience with Master's or 5+ years with Bachelor's.
• Attention to detail and ability to lead/work on concurrent studies.
• Excellent verbal and written communication skills.
• Extensive SAS programming expertise to an advanced level.
• Ability to work independently on the assigned programming tasks.
• Comprehensive knowledge of technical and regulatory requirements.
• Good knowledge of CDISC standards and industry best practices.
• Experience leading studies or activities in clinical trials.
• Lead experience, Stakeholder management -- Oncology TA and Submission experience preferred.

Responsibilities

• Provide statistical programming support and/or lead activities related to the analysis and reporting process at project/study level for clinical development.
• Scope includes clinical study report development, regulatory submissions, commercialization, and data utilization for AstraZeneca products.
• There are many career options for development and progression within the team.

Skills

SAS programming

CDISC standards

Regulatory requirements

Leadership

Communication skills

Clinical trials

Independent work

Education

Bachelor's or Master's in Mathematics/Statistics/CS/Life or Social Sciences

Tools

SAS

Job description

Job Title: Senior Statistical Programmer II * Career Level -- D * Location: Manyata Tech Park, Bangalore * Work Type: Hybrid

Introduction to role: Do you have passion for Programming? Do you consider yourself an SME? Would you like to apply your skills to impact drug development process and regulatory interactions in a company that follows the science and turns ideas into life-enhancing medicines? Then AstraZeneca might be the one for you! Join our team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. With multiple indications and high-quality molecules in all stages of our innovative pipeline, we keep pushing forward to conquer cancer through data, innovation, and evidence-based decisions. About AstraZeneca: AstraZeneca is a global, science-led, patient-focused pharmaceutical company that focuses on the research, development, and commercialisation of prescription medicines. We aim to transform the lives of patients with improved outcomes and a better quality of life. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we 're dedicated to being a Great Place to Work.

Accountabilities: As a Senior Statistical Programmer, you will be working in the Oncology Biometrics Programming department providing statistical programming support and/or leading activities related to the analysis and reporting process at project/study level for the delivery of statistical programming aspects of clinical development. The scope of work includes, but is not limited to, clinical study report development, regulatory submissions, commercialization, and the scientific utilization of our data for AstraZeneca products. There are many career options that you can pursue for your development and progression.

Essential Skills/Experience:

• Bachelor's or Master's (or local equivalent) in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field.
• At least 3 years of industry experience with Master's or 5+ years with Bachelor's.
• Ability to pay attention to detail and lead/work on concurrent studies and activities.
• Excellent verbal and written communication skills and ability to influence team members.
• Extensive SAS programming expertise to an advanced level within clinical drug development.
• Ability to work independently on the assigned programming tasks.
• Comprehensive knowledge of technical and regulatory requirements.
• Good knowledge of CDISC standards and industry best practices.
• Experience leading studies or activities in clinical trials.
• Lead experience, Stakeholder management -- Oncology TA and Submission experience preferred.

Why AstraZeneca:

Here, you will tackle complex, meaningful problems with the support of diverse experts and the momentum of a rich pipeline. You will see your work in countless filings and high-impact studies, and grow through a culture that constructively challenges ideas while celebrating learning. We invest deeply in science and technology, bring different perspectives together to unlock better solutions, and connect every line of code to the lives of people waiting for new options. We value kindness alongside ambition, giving you the room to stretch while helping you deliver work that truly matters. AstraZeneca is a place where courage, curiosity, and collaboration thrive. We make bold decisions driven by patient outcomes, empowering our team to lead at every level. Our collaborative research environment unites academia and industry, expediting breakthroughs in some of the hardest-to-treat cancers. Here, you can build a rewarding career while improving the lives of millions with cancer.

In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We align with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Date Posted 20-Aug-2026

Closing Date 23-Aug-2026