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Tier-1 brand, metro location, mid-level experience increases competition but niche SAS/CDISC skill reduces pool.
Pharma-specific CDISC, regulatory and clinical programming skills limit transferability across industries.
Mandatory SAS/CDISC, clinical-regulatory experience and explicit years requirement create strict shortlisting filters.
Provide statistical programming support and/or lead analysis and reporting activities at the project/study level within clinical development, especially in Oncology Biometrics Programming.
Deliver programming contributions for clinical study report development, regulatory submissions, commercialization, and scientific data utilization for AstraZeneca products.
Manage multiple concurrent studies and ensure 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 2 years of industry experience with a Master’s degree, or 4+ years with a Bachelor’s degree.
Extensive advanced-level SAS programming expertise within clinical drug development.
Knowledge of CDISC standards and regulatory programming requirements.
Experienced in leading studies or activities within clinical trials programming, demonstrating capability to manage and influence study deliverables.
Comfortable working independently on assigned programming tasks and collaborating globally across teams.
Strong attention to detail with ability to multitask and handle concurrent study activities effectively.