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Tier-1 pharma brand and Bangalore metro presence increase competition despite niche SAS/CDISC skill requirements.
Pharma-specific CDISC and regulatory experience limits transferability across industries.
Explicit years plus mandatory SAS, CDISC, and clinical/regulatory experience create high filtering.
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Provide statistical programming support and lead programming activities for oncology clinical trial analysis and reporting at project/study level.
Contribute to clinical study report development, regulatory submissions, commercialization, and scientific data utilization for AstraZeneca products.
Manage multiple concurrent studies with adherence to technical and regulatory programming requirements.
Bachelor’s or Master’s degree in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field.
At least 3 years of industry experience with Master’s degree or 5+ years with Bachelor’s degree in statistical programming or clinical drug development.
Advanced SAS programming expertise and strong knowledge of CDISC standards and industry best practices.
Located in Bangalore with hybrid work model requiring minimum three days per week in office.
Experienced in leading clinical trial statistical programming activities within oncology or pharmaceutical industry contexts.
Able to work independently and manage multiple projects with attention to detail and adherence to global regulatory standards.
Strong communicator with ability to influence and collaborate effectively in a global, cross-functional team environment.