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Niche clinical SAS role reduces applicants, but metro location, mid-level experience, and AstraZeneca brand increase competition.
Highly specialized clinical-trials and regulatory SAS skills limit transferability across industries.
Multiple mandatory clinical SAS, CDISC, oncology TA and years-of-experience requirements enforce strict filtering.
Provide statistical programming support and/or lead programming activities related to analysis and reporting at project/study level in Oncology clinical development.
Deliver statistical programming components for clinical study reports, regulatory submissions, commercialization, and scientific data use for AstraZeneca products.
Lead studies or activities including stakeholder management within the Oncology therapeutic area, 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 industry experience with a Master’s degree or 5+ years with a Bachelor’s degree in relevant domain.
Advanced expertise in SAS programming within clinical drug development.
Experience leading studies or activities in clinical trials, with knowledge of CDISC standards and regulatory requirements in pharma programming.
Demonstrated ability to lead and manage programming activities in Oncology clinical trials and submissions.
Strong stakeholder management experience in Oncology therapeutic area with regulatory submission exposure.
Capable of working independently and multitasking across concurrent studies in a global team environment with detailed focus.