Senior Statistical Programmer I

AstraZeneca GmbH; Bengaluru; Hybrid; INR 1,200,000 - 1,800,000; Full time

Job summary

AstraZeneca is seeking a Senior Statistical Programmer I in Bengaluru on a hybrid schedule. You will join the Oncology Biometrics Programming team, delivering statistical programming support across study analysis and reporting, contributing to regulatory submissions.

The role requires strong SAS expertise, CDISC knowledge, and ability to lead studies while coordinating with global stakeholders. Hybrid work includes in-office three days per week with flexibility.

Qualifications

• Bachelor’s or Master’s in Mathematics, Statistics, CS, Life or Social Sciences or related field.
• At least 3 years of industry experience with Master’s or 5+ years with Bachelor’s.
• Excellent verbal and written communication skills and ability to influence team members.

Responsibilities

• Provide statistical programming support and/or lead activities related to analysis and reporting for clinical development.
• Contribute to clinical study report development and regulatory submissions; work with a global team.

Skills

SAS programming

Regulatory understanding

CDISC standards

Stakeholder management

Leading studies

Communication skills

Detail-oriented

Education

Bachelor’s or Master’s in Mathematics, Statistics, CS, Life or Social Sciences or related field

Local equivalent

Tools

SAS

CDISC

Job description

Job Title: Senior Statistical Programmer I

• 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:

To succeed in this role, you need to be an enthusiastic individual with an understanding of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry. You should have the ability to multitask, collaborate as part of a global team, and have an appetite for solving problems.

• 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.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. 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. Join us in our unique and ambitious world.

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

26-Aug-2026

Closing Date

30-Aug-2026