Job Information
Amgen Biostatistical Programming Manager in Uxbridge, United Kingdom
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 read over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.
BIOSTATISTICAL PROGRAMMING MANAGER
LIVE
What you will do
In this vital role you will support the Center for Observational Research (CfOR) organization by providing programming in SAS, R and SQL to perform data manipulation and analysis of large observational healthcare databases, as well as leading observational study implementation and quality control and leading a team of statistical programmers. In addition, the manager is responsible for staying informed of evolving departmental needs and industry best practices, looking to identify innovative, impactful proposals to increase efficiency and support the organization’s growth strategies. Two positions are available.
Responsibilities
Write, test and perform quality control of SAS, R and SQL programs to perform data manipulation and analysis of large observational healthcare databases to produce analysis datasets and statistical reports
Lead a team of statistical programmers to deliver accurate outputs on time and to specifications
Coordinate with stakeholders to prioritize and manage workflow
Identify potential efficiency improvements and propose solutions
Ensure that the analysis and presentation of data and results are accurate and complete
Adhere to Amgen policies, SOPs and other controlled documents
Efficiently manage project team resources and timelines
Contribute to the development, review and approval of key study-related documents produced by other functions, e.g. Statistical Analysis Plan (SAP), Case Report Forms (CRF), Data Management Plan, etc.
Write, and/or review and approve programming plans
Write, and/or review and approve analysis dataset specifications
Represent the programming function in multidisciplinary team meetings
Contribute to the continuous improvement of programming, CfOR, and Research and Development (R&D)
Write, test and validate department-, product- and protocol-level macros, functions and utilities
Participate in the development and review of CfOR Policies, SOPs and other controlled documents
Participate in study and systems audits by Clinical Quality Assurance (CQA) and external bodies, and respond to audit questions and findings
Interview potential programming candidates
Actively participate in external professional organizations, conferences and/or meetings
Provide input to and participate in intra-departmental and CfOR meetings
Support and mentor junior programmers
Be part of our team
You would be joining the Center for Observational Research (CfOR) organization. The successful candidate will report to a Sr. Manager of Statistical Programming in CfOR’s International Data & Analytic Center (IDAC).
WIN
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:
Bachelors degree or equivalent in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific subject
Extensive SAS or R programming experience for complex data manipulation and analysis
Proven experience with database programming using SQL
Experience with real world healthcare data such as the Clinical Practice Research Datalink (CPRD), German Disease Analyzer, MarketScan, Optum, DRG, PharMetrics, Medicare or other Electronic Medical Records (EMR) databases
Vendor relationship management or related experience with functional service providers
Experience in a regulated environment
Training or experience using the Observational Medical Outcomes Partnership ( OMOP ) common data model
Training or experience with Databricks or other high performance computing environment
Experience with UNIX operating system
Pharmaceutical industry experience
LOCATION Ability to work flexibly from home with regular office work either from our Uxbridge next generation workspace.
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
APPLY NOW
Objects in your future are closer than they appear. Join us.
Careers.amgen.com
Equal Opportunity Statement
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.