Senior Statistical Programmer

7 days ago

Uxbridge, United Kingdom Regeneron Full time
Job Summary

We are seeking a highly skilled Principal SAS Programmer to lead and support all programming activities per the project strategies. The successful candidate will 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.

Key Responsibilities
  1. Programming and QC: Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements.
  2. Data Integration: Integration of data across studies in support of CSS/CSE. Build, lead and maintain the programming specifications for the analysis datasets applying Regeneron tools and methodologies.
  3. Submission Requirements: Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).
  4. Study Team Collaboration: 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.
Requirements
  1. SAS Programming Skills: Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. Knowledge of other programming languages such as R, Python etc.
  2. Pharmaceutical Clinical Development: Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles). Knowledge of regulatory submissions and requirements is a plus.
  3. Education and Experience: MS (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field with 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health-related industry.

Salary Range: $106,173,200.00

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