Biostatistical Programming Associate

Career Category Research 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 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 3 years of statistical programming experience in clinical development environment. Familiarity with drug development life cycle and excellent skills with manipulation, analysis and reporting of clinical trials data Ability to provide quality output and deliverables, in adherence with challenging timelines Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners Ability to work effectively on multiple tasks or projects Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards, with ability to implement the standards 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 In depth knowledge of SAS/STAT packages Prior regulatory submission experience 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 .