Biostatistical Programming Senior Associate
At a glance
Senior Data Science role at Amgen. Hyderabad · full-time.
Pay not stated Data Science salary
dataroles summary, based on the employer's posting.
What you'll do
- Analyze clinical-trial data in SAS or R and prepare results for studies and regulatory filings
- Build and check complex SDTM, ADaM and other datasets covering safety and efficacy
- Produce and validate complex tables, listings and figures for clinical studies
- Write programming specifications and submission documents, keeping validation and tracking records current
- Check data quality through programming and support the Study Lead Programmer as needed
What you bring
- At least four years of statistical programming in a clinical development setting
- A bachelor’s degree or higher in biostatistics, statistics, mathematics, computer science or another related quantitative or scientific field
- Strong SAS/STAT skills and the ability to apply CDISC SDTM standards, with familiarity in ADaM and Define
- You can handle complex clinical-trial data, deliver accurate work to tight timelines and manage several projects
- Clear written and spoken English for collaboration across global, cross-cultural teams
Who this fits
This role suits a hands-on statistical programmer who can manage complex clinical data and contribute across study teams. It is based in Hyderabad, India, and includes support for the Study Lead Programmer.
From the employer
Career Category
Information SystemsJob Description
Biostatistical Programming Senior Associate
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 Senior Associate
What you will do
Let’s do this. Let’s change the world.
Amgen is expanding its global Statistical Programming capabilities, with Amgen India (AIN) playing a key role in supporting integrated delivery across regions. As a Biostatistical Programming Senior Associate, you will perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions.
Key Responsibilities:
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of complex tables, listings, and figures, both safety and efficacy
Prepare statistical programming specifications
Prepare statistical programming related documents for regulatory submissions
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
Interact and collaborate with study team members from other functions globally
Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
This position will be located at Amgen India (Hyderabad).
Win
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a results-oriented, tech-forward programming leader with deep expertise in clinical trial operations and digital transformation.
Basic Qualifications:
BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects, with at least 4 years of statistical programming experience in relevant career statistical programming experience in a clinical development environment.
Familiarity with drug development life cycle and excellent skills with the manipulation, analysis and reporting of complex clinical trial data
Ability to effectively perform complex statistical programming and related tasks
Ability to provide quality output and deliverables in adherence with challenging timelines
Ability to work effectively on multiple tasks or projects across therapeutic areas
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards with strong ability to implement the standards
In depth knowledge of SAS/STAT packages
Familiar with data quality and compliance check tools
Excellent oral and written English communication skills
Preferred Skills:
MSc or higher degree in statistics, biostatistics, mathematics, or related quantitative or scientific subjects
Familiarity with open-source programming tools (R, Python), automation platforms, and emerging technologies in statistical programming
Prior regulatory submission experience for drug approval
Thrive
What you can expect of us
As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.
Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
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