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Tier-1 brand, mid-level experience band, and Bangalore metro increase applicant competition.
Requires pharma-specific CDISC and regulatory experience, limiting cross-industry transferability.
Explicit years requirement plus mandatory SAS/CDISC and regulatory expertise make shortlisting strict.
Provide statistical programming support and/or lead activities related to analysis and reporting for clinical development projects/studies in Oncology Biometrics Programming.
Own programming deliverables tied to clinical study reports, regulatory submissions, commercialization, and scientific data use for AstraZeneca products.
Manage concurrent studies and stakeholder communications, ensuring compliance with 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 industry experience with a Master’s degree, or 5+ years with a Bachelor’s degree in relevant field.
Advanced SAS programming expertise within clinical drug development.
Knowledge of CDISC standards and experience with regulatory submission processes.
Experienced in leading clinical trial programming activities, preferably within Oncology therapeutic area.
Capable of working independently while managing multiple concurrent studies and collaborating within global teams.
Skilled at stakeholder management and influencing cross-functional teams during submission and study delivery phases.