Back
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Strong employer brand and Bengaluru location, but specialized SAS/CDISC skills and seniority limit candidate pool.
High because role requires clinical-statistics, SAS programming and CDISC standards specific to pharma trials.
High because explicit 7+ years requirement plus mandatory SAS, CDISC, and clinical trial expertise.
Lead programming, testing, and documentation of statistical programs for complex studies, including tables, figures, listings, and analysis datasets.
Act as technical team lead for complex projects, managing scope, resources, timelines, and client communications.
Provide advanced technical expertise, develop programming specifications, ensure quality control, and mentor statistical programming staff.
Bachelor's degree in Maths, Computer Science, Statistics or related field with 4 years relevant experience OR Master's degree with 3 years relevant experience.
Typically requires 7+ years of prior relevant experience.
Advanced knowledge of statistics, clinical drug development processes, and programming languages like Base SAS, SAS Graph, and SAS Macro Language.
Advanced knowledge of relevant Data Standards such as CDISC/ADaM/SDTM.
Experienced in handling complex statistical programming projects independently with technical team lead responsibilities.
Skilled in interpreting project requirements and collaborating closely with statisticians and clinical teams.
Demonstrates strong leadership in applying programming best practices, team mentoring, and resource management within clinical research context.