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Tier-1 employer, mid-level experience requirement, and metro location increase qualified applicant competition.
Clinical-trial SAS statistical programming is highly domain-specific and not easily transferable across industries.
Explicit years plus mandatory SAS clinical programming skills and regulated-study experience make screening highly stringent.
Develop and coordinate programming solutions for complex statistical studies including tables, figures, listings, and derived datasets.
Lead and provide advanced technical expertise on statistical programming projects, including training and guiding junior staff.
Manage project scope, budget, resource forecasting, and act as statistical team lead for single or multiple complex studies.
Master's degree in Computer Science or related field with 3 years relevant experience OR Bachelor's degree with 4 years relevant experience, or equivalent combination of education and experience.
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language.
Knowledge of statistics, programming, and clinical drug development process.
Work Experience Required: 3-4 years relevant experience depending on educational qualification.
Experienced in handling complex statistical programming projects with demonstrated leadership in managing study deliverables.
Capable of performing project management duties including scope, budget, and resource estimation for clinical research studies.
Strong technical proficiency in SAS programming and ability to coordinate multiple tasks and teams in a clinical research environment.