Senior Manager, Real-World Data Research
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Working with Us Challenging. Meaningful. Life‑changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams. Take your career farther than you thought possible.
Position Purpose
As part of the Real‑world Data Research (RWDR) team, you will work with a collaborative team in an inclusive and supportive environment. You will be an individual contributor responsible for performing non‑interventional research projects in support of key customer groups including medical and health economics and outcomes research (HEOR) and others for International Markets (Europe, APAC and rest of world). Project work includes identification of appropriate data sources, input into the study design, overseeing programming, analysis and summary of data and collaboration with stakeholders on interpretation and presentation of results. You will have the opportunity to contribute towards team/department initiatives with goals of optimizing and innovating RWD research.
Key Responsibilities
* Conduct thorough and careful analysis of data, including
* Overseeing programming of the appropriate statistical analyses
* Delivering results to customers in appropriate formats
* Assisting with follow‑up questions and interpretation of results
* Assist with identification of appropriate data sources for the research objectives
* Actively engage with customers on study concept development, protocol and statistical analysis plan (SAP) writing, and dissemination (e.g., abstracts, manuscripts)
* Communicate the results of analyses conducted effectively orally and in writing
* Manage complex work environment, balancing demands from multiple customers to execute projects
* Make sound scientific decisions based on a balance of data, analysis, and experience
* Work seamlessly in flexible manner across diverse therapeutic areas and assets, study designs and data sources
Qualifications & Experience
* Advanced degree in a quantitative discipline such as biostatistics, epidemiology or a related field
* Pharmaceutical and/or Epidemiology/ Outcomes Research experience
Required Knowledge and Competencies
* Deep understanding of secondary and/or primary patient data sources and demonstrated ability in using such data sources for real‑world research and analysis purposes
* Demonstrated abilities to analyze observational data for pharmaco‑epidemiology, outcomes research, and market research
* Ability to effectively manage research projects
* Ability to effectively communicate a study's objectives, methods, and findings
* Proficient in SAS/R programming to execute these studies; ability to program more advanced analytics and use of GitHub is a plus
* Ability to write (or critically review) the scientific content and analytical sections of protocols, statistical analysis plans, final reports and dissemination
* Ability to apply statistical methods to real‑world studies (e.g., survival analysis, logistic/multivariate regression); knowledge on machine learning methods (e.g., clustering, prediction, NLP) is a plus
Equal Employment Opportunity – Bristol Myers Squibb is an Equal Opportunity Employer. The company is committed to a diverse workforce and encourages people from all backgrounds to apply. EEO is mandated by law. We do not discriminate based on race, color, national origin, sex, sexual orientation, gender identity, age, disability, or any other protected characteristic. For more information, visit careers.bms.com/eeo.
Disability Confident Employer – We provide reasonable accommodations for qualified individuals with disabilities. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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