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Tier-1 employer, mid-level requirement, and metro location create high applicant competition.
Specialized clinical statistical programming (SAS, CDM, TFLs) limits cross-industry transferability.
Explicit 5-year requirement plus mandatory SAS stack and clinical programming skills increases filter strictness.
Plan and coordinate development of integrated statistical programming solutions for complex studies, including programming, testing, and documentation of statistical tables, figures, and listings.
Provide advanced technical expertise and leadership as statistical team lead for single or multiple complex studies, including managing project scope, resources, budget, and forecasts.
Develop and validate new process technologies, macros, applications, and provide training and consulting services to internal teams and external clients.
Master's or Bachelor's Degree in Computer Science or related field with 5 years relevant experience, or equivalent combination of education, training, and experience.
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language programming.
Knowledge of statistics and clinical drug development processes.
Work Experience Required: At least 5 years relevant experience.
Experienced in handling complex statistical programming projects with leadership responsibilities including team lead and project management roles.
Demonstrates strong organizational skills with ability to manage multiple tasks and projects under budget and scope constraints.
Comfortable providing technical consulting and training to other staff and clients, implying excellent communication and interpersonal skills.