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Strong employer brand plus metro location and mid-level role balanced by niche CDISC/SAS specialization.
Role requires specialized clinical trial, CDISC and regulatory expertise, limiting cross-industry transferability.
Explicit 4+ years, mandatory SAS/CDISC and regulated submission experience make filters stringent.
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Perform hands-on statistical programming for complex clinical trial data analysis and regulatory submissions using SAS and/or R.
Create and validate complex clinical trial datasets (SDTM, ADaM) and statistical outputs (tables, listings, figures) for safety and efficacy.
Prepare programming specifications, maintain validation documentation, and collaborate globally with cross-functional teams; support Study Lead Programmer tasks or act as backup.
Bachelor's degree in biostatistics, statistics, mathematics, computer science, or related quantitative/scientific field.
At least 4 years of statistical programming experience in a clinical development environment.
Working knowledge of CDISC SDTM standards, familiarity with ADaM and Define standards, and proficiency in SAS/STAT packages.
Location requirement: Amgen India (Hyderabad).
Experienced in clinical trial operations with strong skills in manipulating and analyzing complex clinical trial data.
Ability to deliver quality work within challenging timelines and work on multiple projects across therapeutic areas.
Comfortable working effectively in a globally dispersed, cross-cultural team environment.