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Tier-1 employer and Bangalore location increase density, though SAS/CDISC specialization narrows candidate pool.
Clinical-trial SAS and CDISC programming skills are highly domain-specific and not easily transferable.
Requires 7+ years, mandatory SAS and CDISC/ADaM/SDTM expertise, and advanced clinical programming skills.
Develop, test, and document complex statistical programming solutions for tables, figures, listings, and analysis datasets.
Lead and manage programming projects including scoping, resource assignment, timeline management, and client communication.
Provide technical leadership, mentoring, and internal consulting for statistical programming teams on complex studies.
Bachelor's degree in Mathematics, Computer Science, Statistics, or related field with 4 years relevant experience, or Master's with 3 years relevant experience.
Typically requires 7+ years of prior relevant experience.
Advanced knowledge of statistics, statistical programming (Base SAS, SAS Graph, SAS Macro), and clinical drug development process.
Advanced knowledge of relevant Data Standards such as CDISC/ADaM/SDTM.
Experienced in independently handling complex statistical programming projects with a leadership role.
Strong communicator able to negotiate timelines and directly liaise with statisticians and clinical teams.
Skilled in establishing programming standards and mentoring team members for process improvement.