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Observational research manager

Uxbridge
Amgen
Research manager
€60,000 a year
Posted: 20h ago
Offer description

About the Role

The Observational Research Manager (ORM)/Epidemiologist role is part of the Data & Analytics Center (DAC) within the Center of Observational Research (CfOR). The DAC ORM/Epidemiologist is responsible for performing analyses on Amgen's Real-World Data (RWD) assets, including writing Statistical Analysis Plans (SAPs), developing medical code lists for studies, guiding data analysts to explore large healthcare databases, and interpreting study results and outputs. Prior experience with large databases such as CPRD and HES is strongly desired, as is experience in SAS, R, or other statistical software.


Responsibilities

* Write Statistical Analysis Plans (SAPs).
* Contribute to projects using RWD assets.
* Guide analysts to explore and analyze RWD.
* Contribute to research strategy within the product team and epidemiology therapeutic area.
* Provide input into epidemiology department meetings.
* Stay abreast of the latest developments in Epidemiology, Drug Development, Healthcare RWD and contribute to the field.
* Promote epidemiologic awareness.
* Promote understanding and use of RWD and epidemiologic methods.
* Communicate significant scientific information to a variety of audiences.


Qualifications

* Doctorate in Epidemiology, Statistics, or related discipline with strong epidemiologic content.
* Experience in epidemiologic research.
* Experience working with observational data.
* Experience communicating epidemiologic information (written and oral).
* Knowledge of SAS, R, or other statistical software.
* Strong written, verbal communication, organization, and time‑management skills.


Preferred Qualifications

* MSc in Epidemiology, Statistics, or related discipline with strong quantitative content.
* Experience within the Cardiovascular or Obesity therapeutic area.
* Experience in design, execution, and analysis of epidemiology studies within pharmaceutical or public health settings.
* Experience supporting drug development research.
* Experience with large databases such as CPRD and HES.
* Experience in epidemiological project planning & management.
* Experience working in multidisciplinary teams.
* Record of publication in peer‑reviewed journals.
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