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Tier-1 employer and Bangalore location increase applicant density, though specialized clinical SAS skills limit breadth.
Strong CDISC/ADaM/SDTM and clinical trial domain specificity limits cross-industry transferability.
Explicit 7+ years requirement plus mandatory SAS, CDISC/ADaM/SDTM skills and leadership make filters strict.
Lead the programming, testing, and documentation of statistical tables, figures, listings, and analysis datasets for complex studies.
Serve as technical team lead, managing programming scope, resource assignments, project timelines and communication with internal and client teams.
Provide internal consulting, develop programming specifications, promote standards/SOPs, and mentor Statistical Programming team members.
Bachelor's degree in Mathematics, Computer Science, Statistics, or related field with 4 years relevant experience, OR Master's degree with 3 years experience.
Typically requires 7+ years of prior relevant experience.
Advanced knowledge of statistics, programming (Base SAS, SAS Graph, SAS Macro), and clinical drug development process.
Advanced knowledge of data standards such as CDISC/ADaM/SDTM.
Experienced in managing and delivering integrated programming solutions for complex clinical studies with leadership responsibility at team/staff level.
Strong capability in client communication and negotiation to clarify requirements and manage timelines.
Technically advanced with broad knowledge of statistical programming, clinical development, and regulatory data standards to independently drive project solutions.