Biostatistical Programming Manager
Amgen · India - Hyderabad
Free account: apply link, HR contact and an AI-written cold email
Amgen · India - Hyderabad
Free account: apply link, HR contact and an AI-written cold email
Career Category Research Job Description Biostatistical Programming Manager HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. 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 for study programming team Coordinate and monitor data issue reporting and resolution Coordinate with other SLPs to providing consistent deliverables across studies within a product Manage technical aspects of project (e.g., create/manage computing environment, lookup tables, etc.) Provide training and guidance to other programmers Assume some product level responsibilities as delegated by Global Programming Lead (GPL) and/or Programming Execution Lead (PEL). This position will be located at Amgen India (Hyderabad). Win
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