Career Category
Clinical Development
Job Description
Biostatistical Programming Manager
What you will do
Let’s do this. Let’s change the world.
Amgen is expanding its Global Statistical Programming (GSP) capabilities, with Amgen India (AIN) playing a key role in supporting integrated delivery across regions. As a Biostatistical Programming Manager, you will serve as the Study Lead Programmer (SLP) for one or more studies and lead a team of statistical programmers to support all statistical programming activities within a study. You may also support regulatory submissions.

Key Responsibilities:
Lead one, or more than one, study/project end to end and assume all the responsibilities of Study Lead Programmer
Set the programming strategy for the studies and projects and ensure timelines, quality, and compliance of all deliverables
Lead and manage specific programming tasks (e.g., all programming related activities of an integrated analysis that involves multiple studies for regulatory submissions) assigned to the team




Participate in establishing the programming scope for a deliverable with the statisticians and the study team
Participate in establishing detailed timelines that will ensure timely delivery of programming deliverables for a study or project
Create and maintain programming related specifications (e.g., SDTM and ADaM) for the studies/projects
Represent GSP at the Clinical Study Team (CST)
Attend meetings for, and provide programming input into, cross-functional study start-up activities, including but not limited to CRF development, database specifications review, database development, IVRS specification review, data quality check specifications
Initiate cross-functional team meetings as necessary
Perform significant hands-on statistical programming, particularly for those most challenging deliverables
Manage individual programmer work assignments to ensure timely, high-quality deliverables
Provide technical leadership and guidance f

📌 Biostatistical Programming Mgr Hyderabad (India)
🏢 AMGEN
📍 India