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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.
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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 6 years of statistical programming experience in clinical development environment.
Thorough understanding of clinical trial processes, from data collection to analysis reporting
Proven record of superior statistical programming and problem-solving skills within clinical development environment
Prior experience and ability to lead and manage statistical programmers in successful and timely completion of all programming related activities (including preparing data and programming specifications) for a study end-to-end
In-depth knowledge on latest CDISC SDTM, ADaM, and Define standards along with strong ability to implement all aspects of those standards
Advanced analysis and reporting skills in SAS, including SAS/STAT packages, among others
Experience in data quality and compliance check tools
Excellent project management skills and ability to lead multiple projects effectively
Excellent oral and written English communication skills
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
Willingness and ability to provide guidance to team members on technical and process questions
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
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
Developing innovative medicines to fight serious diseases.
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Senior · 6+ years experience
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