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Tier-1 employer, mid-level experience requirement, and metro Bangalore location increase applicant competition.
Clinical trial statistical programming requires domain-specific regulatory and SAS skills, limiting cross-industry transferability.
Explicit 5+ years requirement plus mandatory SAS, CDISC and regulatory experience make filters strict.
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Provide statistical programming support and/or lead statistical programming activities for clinical study analysis and reporting at project/study level in Oncology Biometrics Programming.
Deliver statistical programming aspects related to clinical study reports, regulatory submissions, commercialization, and scientific data utilization for AstraZeneca products.
Lead or work concurrently on multiple studies, managing programming tasks independently while ensuring compliance with technical and regulatory 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 related pharmaceutical/healthcare field.
Extensive advanced level SAS programming expertise within clinical drug development.
Working hybrid from Bangalore office with minimum 3 days onsite per week as stated.
Experienced in Oncology therapeutic area with stakeholder management and clinical trial submission exposure preferred.
Ability to lead studies or activities in clinical trials with comprehensive knowledge of CDISC standards and regulatory programming requirements.
Capable of managing multiple concurrent programming projects independently in a global team environment, demonstrating strong problem-solving and communication skills.