Career Category
Clinical
Job Description
Biostatistical Programming 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.
Statistical Programming 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 Associate, you will perform hands on statistical programming activities to support statistical data analysis of phase 1 to 4 clinical studies and regulatory submissions.
Responsibilities:
Analysis and reporting of clinical trial data using SAS and/or R
Creation and validation of SDTM, ADaM, and other analysis datasets, both safety and efficacy
Creation and validation of tables, listings, and figures, both safety and efficacy
Maintain tracking and validation documentation
Collaborate with cross-functional team and create and/or validate programs for checking data quality
Interact and collaborate with study team members from other functions globally
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 skilled 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 3 years of statistical