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Tier-1 brand, Bengaluru metro location, and mid-level experience increase applicant density.
Highly industry-specific clinical trial programming skills reduce transferability across industries.
Explicit years plus mandatory SAS, CDISC, and regulatory experience enforce strict filtering.
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Lead and provide advanced statistical programming support for oncology clinical studies, including analysis and reporting for clinical study reports and regulatory submissions.
Manage multiple concurrent programming tasks and collaborate with global teams to ensure regulatory compliance and data quality for AstraZeneca products.
Influence stakeholder management within Oncology therapeutic area, contributing to clinical development and commercialization efforts.
Bachelor's or Master's degree in Mathematics, Statistics, Computer Science, Life or Social Sciences, or related field.
Minimum 3 years of industry experience with a Master's degree or 5+ years with a Bachelor's degree in statistical programming or related fields.
Advanced SAS programming expertise specific to clinical drug development and familiarity with CDISC standards and regulatory requirements.
Experience leading studies or activities, including stakeholder management within Oncology therapeutic area and submission experience.
Experienced in managing complex and concurrent oncology clinical trial programming deliverables with strong attention to detail.
Capable of working independently and leading programming activities in a regulated pharmaceutical environment focused on oncology.
Able to effectively communicate and influence multidisciplinary global teams and stakeholders in a fast-paced clinical development setting.