Back
Strong employer brand and metro location increase competition despite niche CDISC/SAS specialization.
Role requires clinical trial and CDISC/SAS expertise, limiting cross-industry transferability.
Mandatory six-plus years and specific CDISC/ADaM and SAS expertise create strict screening filters.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Lead one or more clinical studies end-to-end as Study Lead Programmer, managing all statistical programming activities to ensure quality, compliance, and timelines.
Set programming strategy, create and maintain programming specifications (e.g., SDTM, ADaM), and participate in study start-up activities across cross-functional teams.
Manage and guide a team of statistical programmers, provide technical leadership, coordinate data quality issue resolution, and support regulatory submission programming tasks.
Bachelor's degree in biostatistics, statistics, mathematics, computer science, or related quantitative/scientific field.
At least 6 years of statistical programming experience in clinical development environment.
In-depth knowledge of CDISC SDTM, ADaM, and Define standards and advanced SAS programming skills including SAS/STAT packages.
Location requirement: Amgen India (Hyderabad).
Experienced leader in clinical statistical programming with ability to manage multiple projects and teams globally.
Strong expertise in clinical trial processes from data collection through analysis and reporting with regulatory submission experience.
Technically skilled in SAS programming, data quality/compliance tools, and knowledgeable about automation platforms and emerging programming technologies.