Mindblowing Jobs

Senior Statistical Programmer I

By Admin · Biostatistics & Statistical Programming

BANGALORE (IN)HYBRIDPOSTED: 8/26/2026
PHARMAFull-time
HIRING ORGANIZATIONASTRAZENECAPharmaceuticals / Biopharmaceuticals / Healthcare
AstraZeneca

ROLE DEFINITION & RESPONSIBILITIES

Core Responsibilities

Provide statistical programming support and/or lead activities related to analysis and reporting at project/study level within Oncology Biometrics Programming. Support delivery of statistical programming activities across clinical development, including clinical study reports, regulatory submissions, commercialization, and scientific use of AstraZeneca data.

Technical & Domain Responsibilities

Perform advanced SAS programming within clinical drug development.
Apply technical and regulatory requirements relevant to pharmaceutical and healthcare programming.
Work on concurrent studies and activities while maintaining attention to detail and quality.
Apply knowledge of CDISC standards and industry best practices.
Work independently on assigned statistical programming activities.
Support or lead clinical-trial studies and programming activities.
Contribute to analysis and reporting processes supporting clinical development and regulatory interactions.

Stakeholder & Collaboration

Collaborate with global teams and cross-functional stakeholders.
Communicate effectively with team members and influence stakeholders when appropriate.
Manage multiple priorities and solve programming and study-related problems.
Support oncology projects and regulatory submission activities where applicable.

Qualifications

Bachelor's or Master's degree or local equivalent in Mathematics, Statistics, Computer Science, Life Sciences, Social Sciences, or a related field.
At least 3 years of industry experience with a Master's degree or 5+ years with a Bachelor's degree.
Strong SAS programming expertise at an advanced level within clinical drug development.
Knowledge of technical and regulatory requirements.
Good understanding of CDISC standards and industry best practices.
Experience leading studies or activities in clinical trials.

Work Model

The position is based at Manyata Tech Park, Bangalore, with a hybrid working model. AstraZeneca states that employees generally work a minimum of three days per week from the office while retaining flexibility.

REQUIRED VERIFIED SKILLS

SAS Programming
Clinical Drug Development
Statistical Programming
CDISC
Clinical Trials
Regulatory Requirements
Clinical Study Reporting
Regulatory Submissions
Oncology Biometrics
Data Analysis
Statistical Analysis
Pharmaceutical Industry
Healthcare Programming

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting

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.

TEAM SIZE: 89,000+ employees
INDUSTRY: Pharmaceuticals / Biopharmaceuticals / Healthcare
RECOMMENDED TRAINING
1/5
The Fundamentals of Regulatory Affairs

The Fundamentals of Regulatory Affairs

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.