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Strong pharma brand and Bangalore location increase applicant density despite specialized SAS/CDISC skill requirement.
Requires clinical trial domain knowledge and CDISC/SAS expertise, limiting cross-industry transferability.
Explicit years requirement, mandatory SAS/CDISC expertise, and regulatory experience enforce strict shortlisting.
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Provide statistical programming support and/or lead programming activities for clinical development projects/studies in Oncology.
Responsible for clinical study report development, regulatory submissions, and data utilization for AstraZeneca products.
Work involves applying advanced SAS programming expertise within the analysis and reporting processes at project/study level.
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 a Master’s degree, or 5+ years with a Bachelor’s degree in relevant fields.
Extensive advanced SAS programming skills within clinical drug development.
Hybrid work location requirement at Manyata Tech Park, Bangalore (minimum three days per week onsite).
Experienced in leading programming activities or studies within clinical trials, particularly oncology domain preferred but not explicitly stated.
Strong knowledge of technical and regulatory requirements related to statistical programming in pharmaceutical or healthcare industry.
Ability to work independently on assigned programming tasks while managing multiple concurrent studies or activities.