Principal Statistical Programmer

$106,200 - $173,200/Yr

Regeneron Pharmaceuticals - Uxbridge, MA

posted 5 months ago

Full-time - Senior
Uxbridge, MA
11-50 employees
Professional, Scientific, and Technical Services

About the position

The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal partnering functions, collaborators, and external functional service providers to ensure all the programming results are delivered in a timely manner with high quality. In this role, a typical day might include the following: Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Integration of data across studies in support of CSS/CSE. Build, lead and maintain the programming specifications for the analysis datasets using Regeneron tools and methodologies. Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents). Work 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. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.

Responsibilities

  • Lead and support programming activities for clinical studies and regulatory submissions.
  • Support and/or lead programming and quality control of analysis datasets and TFLs.
  • Integrate data across studies in support of CSS/CSE.
  • Build, lead, and maintain programming specifications for analysis datasets.
  • Support the creation and validation of submission requirements such as annotated CRF and data export files.
  • Work in a multidisciplinary study team to provide support for analysis and reporting of clinical trials.
  • Develop and provide training for applications and standard tools.

Requirements

  • MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field.
  • 5+ years of programming experience in processing clinical trial data in the biotechnology, pharmaceutical or health-related industry.
  • Proficiency in SAS programming skills in a clinical data environment.
  • Knowledge of other programming languages such as R and Python.
  • Good knowledge of pharmaceutical clinical development and understanding of statistical concepts and clinical trial principles.

Nice-to-haves

  • SAS certificates are a plus.
  • Knowledge of regulatory submissions and requirements is a plus.

Benefits

  • Health and wellness programs
  • Fitness centers
  • Equity awards
  • Annual bonuses
  • Paid time off for eligible employees
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