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Tier-1 brand plus mid-level experience amplifies competition despite niche clinical SAS specialization.
Clinical biostatistics and IRT/SAS expertise are industry-specific, so background fit sensitivity is high.
Explicit 4+ years clinical SAS programming and IRT/domain requirements create high shortlisting strictness.
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Create and deliver Participant and Investigational Product (IP) randomization lists according to specifications.
Develop, validate, and verify SAS programs to confirm randomization and dose decisions from an Interactive Response Technology (IRT) system during clinical trials.
Manage IRT data transfer activities, including acting as gatekeeper for data entering secure Amgen sFTP locations, ensuring compliance with study blind procedures and documentation.
Bachelor s degree or higher in biostatistics, statistics, mathematics, computer science, or related field.
At least 4 years of statistical programming experience in a clinical development environment.
Experience with biostatistical programming using SAS version 8.2 or higher; knowledge of R or Python is a plus.
Work Experience Required: Minimum 4 years in clinical development statistical programming.
Experienced in clinical trial programming with strong SAS programming and validation skills relevant to randomization and blinding processes.
Familiar with Interactive Response Technology (IRT) systems and clinical data transfer protocols, especially within global randomization and blinding contexts.
Has participated in project planning, process improvement, and cross-functional teamwork within drug development environments.