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Regeneron Pharmaceuticals, Inc

Senior Statistical Programmer

Regeneron Pharmaceuticals, Inc, Jackson, Mississippi, United States,


A senior statistical programmer provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines.In this role, a typical day might include the following:Assisting in providing guidance in implementing and executing the programming and project standards.Evaluating and developing study requirements and validation plans.Designing and testing program logic, coding programs, program documentation, and preparation of programs.Overseeing projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses.Meeting statistical ad-hoc requests of senior management.Providing documentation and consistent maintenance of code, logs, and output in a regulated environment.This role may be for you if you have:Experience as a support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements.Experience in the integration of data across studies in support of CSS/CSE.Ability to create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.Experience in supporting creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).Experience working in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch, and annual reports.Capability to develop and provide department training for applications and standard tools developed by the department functions group.To be considered for this opportunity you must have:MS (or BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health-related industry.Salary Range (annually)$90,700.00 - $148,100.00

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