Clinical Data Analyst Manager

1 day ago


Uxbridge, United Kingdom Regeneron Pharmaceuticals, Inc Full time
Responsibilities
  • Lead programming support within multiple studies/projects in various study activities to ensure timely and high-quality programming deliverables in assigned projects and areas.
  • Develop and maintain programming documentation and specifications following programming standards and processes.
  • Support global regulatory authority submissions including preparing programming deliverables for submission and working closely with partnering functions to address health authority requests.

This role may be for you if you have:

  • Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills.
  • Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles).
  • SAS (Base, Stat, Macro, graph); SAS certificates a plus.

To be considered for this opportunity, you must have:

A MS (or BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical, or health-related industry. Estimated salary: $120,000 - $180,000 per annum based on location and experience.


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