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Tier-1 pharma brand plus Bangalore metro and mid-level experience increases applicant competition.
Requires clinical trial, CDISC and regulatory expertise, limiting transferability across other industries.
Explicit years plus mandatory SAS, CDISC and regulatory experience make screening highly strict.
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Provide statistical programming support and lead programming activities related to analysis and reporting at project/study level within Oncology clinical development.
Deliver clinical study report programming, regulatory submission support, commercialization, and scientific data utilization for AstraZeneca products.
Lead stakeholder management and programming activities aligning with technical and regulatory standards including CDISC and industry best practices.
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.
Advanced SAS programming expertise specific to clinical drug development.
Work Location: Hybrid role based in Manyata Tech Park, Bangalore.
Experienced in leading clinical programming studies or activities, preferably with Oncology Therapeutic Area and regulatory submission exposure.
Strong knowledge of technical and regulatory requirements, including CDISC standards and industry best practices.
Able to multitask and independently handle concurrent studies, with effective stakeholder management skills in a global team environment.