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Protocol Intelligence
Data-driven signals on your job's competitivenessTier-1 CRO brand and metro Hyderabad increase candidate interest, though SAS clinical specialization narrows pool.
Clinical trial SAS programming is niche to pharma/CRO, limiting cross-industry transferability.
Explicit 7/8 years and mandatory Base SAS/statistical programming skills create strict screening filters.
Job Description
Structured overview of role & requirementsAbout This Role
Lead and coordinate programming, testing, and documentation of statistical programs for complex clinical studies including analysis databases and quality control checks.
Develop and implement integrated programming solutions, process technologies, macros, and applications supporting statistical programming needs.
Manage project scope, resource forecasts, budgets, and provide training and technical leadership at the statistical team lead level for single or grouped complex studies.
Minimum Requirements
Master's degree in Computer Science or related field with 7 years relevant experience OR Bachelor's degree with 8 years relevant experience OR equivalent education and experience.
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language required.
Experience with statistics, programming, and clinical drug development processes.
Work Experience Required: 7-8 years as specified, no notice period explicitly mentioned.
Ideal Candidate Profile
Experienced in leading complex statistical programming projects and integrating multi-study databases.
Strong technical expertise in SAS programming and clinical data analysis with ability to manage budgets and forecasts.
Capable of training and guiding junior staff while delivering advanced solutions independently to internal and external clients.