Senior Biostatistician: Design, Analysis & Regulatory Support

Alexion Pharmaceuticals, Inc.

Boston (MA)

Presencial

USD 87.000 - 130.000

Jornada completa

Hace 3 días
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Ventajas ofrecidas por este puesto de trabajo

Incentives (short-term bonuses)
Health, dental and vision coverage
Retirement plan
Paid time off

Descripción de la vacante

Alexion Pharmaceuticals, Inc. seeks a Senior Biostatistician, Biostatistics to provide study-level statistical support under supervision.

You will work on set-up, conduct, analysis, and reporting for standard studies, including validation and interpretation of results. The role involves applying modelling and simulation to inform design decisions, developing SAPs, producing analyses and graphics for preclinical and clinical studies, and supporting regulatory submissions while contributing to

Formación

  • 1+ years of experience with MSc/PhD in Statistics, Mathematics (containing a substantial statistical component)
  • Programming knowledge and experience (SAS or R preferred)
  • Strong communication skills
  • Good time management and ability to work under pressure

Responsabilidades

  • Statistical support for standard study design and interpretation
  • Statistical validation activities
  • Analysis of information to inform design decisions and decision criteria
  • Application of modelling and simulation to inform study design
  • Development of a Statistical Analysis Plan
  • Production of analysis, graphics and tables for studies or publications
  • Communication of results of standard studies
  • Support for regulatory submissions
  • Contribute to improvement of methodology and best practices

Conocimientos

SAS/R programming
Communication skills
Time management
Self-awareness

Educación

MSc/PhD in Statistics/Mathematics

Herramientas

SAS
R

Descripción del empleo

Alexion Pharmaceuticals, Inc. seeks a Senior Biostatistician, Biostatistics to provide study-level statistical support under supervision.

You will work on set-up, conduct, analysis, and reporting for standard studies, including validation and interpretation of results. The role involves applying modelling and simulation to inform design decisions, developing SAPs, producing analyses and graphics for preclinical and clinical studies, and supporting regulatory submissions while contributing to

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