PHARMAFull-time
Statistical Programmer II
BANGALORE (IN)HYBRIDPOSTED: 9/10/2026
PHARMAFull-time
HIRING ORGANIZATIONASTRAZENECAPharmaceuticals / Biopharmaceuticals / Healthcare
ROLE OVERVIEW
Provide advanced statistical programming support for oncology clinical development, contributing to clinical study reports, regulatory submissions, commercialization, and evidence generation for AstraZeneca medicines.
ROLE DEFINITION & RESPONSIBILITIES
- •Provide statistical programming support and lead activities for clinical development studies
- •Develop and support analysis and reporting deliverables at project or study level
- •Contribute to clinical study reports and regulatory submission activities
- •Apply advanced SAS programming expertise to clinical drug development
- •Ensure programming activities comply with technical, regulatory, CDISC, and industry requirements
- •Lead or contribute to concurrent clinical trials and programming activities
- •Collaborate with global teams and communicate technical information effectively
- •Solve programming and study-level problems while working independently
Reporting Hierarchy: Reports to/works within the Oncology Biometrics Programming organization; collaborates with statisticians, clinical development teams, regulatory stakeholders, and global programming teams
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's or Master's degree in Mathematics, Statistics, Computer Science, Life Sciences, Social Sciences, or related field
- At least 2 years of industry experience with a Master's degree or 4+ years with a Bachelor's degree
- Advanced SAS programming expertise in clinical drug development
- Knowledge of technical and regulatory programming requirements
- Good knowledge of CDISC standards and industry best practices
PREFERRED QUALIFICATIONS
- •Experience leading studies or activities in clinical trials
- •Oncology clinical development experience
- •Experience supporting regulatory submissions and clinical study reports
- •Strong global-team collaboration and stakeholder influence skills
REQUIRED VERIFIED SKILLS
SAS programming
clinical drug development
statistical programming
CDISC
clinical trials
regulatory requirements
clinical data analysis
clinical reporting
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Health and employee benefits, paid leave, retirement benefits, professional development and other company-standard benefits
No salary range or bonus/equity information is disclosed in the provided posting. Compensation should be confirmed directly with AstraZeneca during recruitment.
ORGANIZATION CONTEXT & CULTURE
AstraZeneca is a global, science-led, patient-focused pharmaceutical company focused on researching, developing, and commercializing prescription medicines, with a major focus on innovative oncology treatments.
TEAM SIZE: 50,000+ employees
INDUSTRY: Pharmaceuticals / Biopharmaceuticals / Healthcare
Culture: Science-led, patient-focused, collaborative, inclusive, and innovation-oriented culture emphasizing curiosity, courage, learning, and evidence-based decision-making.
EXPECTED CAREER ROADMAP
The role offers progression into Senior Statistical Programmer, Lead Statistical Programmer, programming project leadership, biometrics programming management, or specialized clinical development programming roles.
APPLICATION ADVISORY
Emphasize advanced SAS programming experience in clinical drug development; clearly demonstrate CDISC knowledge and clinical trial programming; highlight experience with regulatory submissions and clinical study reports; quantify studies or programming activities led; showcase oncology experience if applicable; demonstrate independent working ability, attention to detail, and collaboration across global teams.
RECOMMENDED TRAINING
1/2
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