AstraZeneca

drug development

SeniorStatisticalProgrammer

India FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Statistical Programmer at AstraZeneca. Skills: SAS programming, statistical programming. providing statistical programming support. leading activities related to the analysis and reporting process at project/study level”

What You'll Achieve.

impact the drug development process and regulatory interactions; eliminate cancer as a cause of death; conquer cancer through data, innovation, and evidence-based decisions; deliver six new molecular entities by 2030; expediting breakthroughs in some of the hardest-to-treat cancers; improving the lives of millions with cancer

Industry & Context.

drug development

What They're Looking For.

Must Have

Bachelor’s or Master’s (or local equivalent) degree 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 degree, 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 procedures

Nice to Have

Experience leading studies or activities in clinical trials

What You'll Do.

providing statistical programming support

leading activities related to the analysis and reporting process at project/study level

clinical study report development

regulatory submissions

scientific utilization of our data for AstraZeneca products

How You'll Work.

Team & Collaboration

work on concurrent studies and activities; ability to influence team members; in-person working gives us the platform we need to connect, work at pace and challenge perceptions; balance the expectation of being in the office while respecting individual flexibility; collaborative research environment unites academia and industry

Communication Scope

Excellent verbal and written communication skills

Process & Methodology

lead/work on concurrent studies and activities, Experience leading studies or activities in clinical trials

Full Job Description

## Job Title: Senior Statistical Programmer I Introduction to role: Do you have a passion for programming? Are you an expert in your field? Would you like to apply your skills to impact the 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. ## Accountabilities: As a Senior Statistical Programmer, you will work within the Oncology Biometrics Programming department, providing statistical programming support and leading activities related to the analysis and reporting process at project/study level. Your responsibilities will include clinical study report development, regulatory submissions, commercialization, and the scientific utilization of our data for AstraZeneca products. There are numerous career paths available for your development and progression. ## Essential Skills/Experience: * Bachelor’s or Master’s (or local equivalent) degree 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 degree * 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 procedures * Experience leading studies or activities in clinical trials When we put unexpected teams

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