Manager, Statistical Programming

Bristol Myers Squibb

Uxbridge, United Kingdom
On-site
Sas programming for derived datasets
Clinical data structure understanding
Cdisc standards knowledge
Bristol Myers Squibb is seeking a Manager of Statistical Programming to provide expert programming support for clinical project teams, facilitating the development and regulatory approval of products. The ideal candidate will have a strong background in statistical programming, particularly with SAS, and experience in the pharmaceutical industry

Job Summary

  • The Manager, Statistical Programming provides comprehensive programming expertise to clinical project teams to support the development, regulatory approval and market acceptance of Bristol Myers Squibb (BMS) products.
  • This position is primarily responsible for the design, development and implementation of technical solutions for integrating, analyzing and reporting clinical data.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits, services and programs.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager of Statistical Programming to provide expert programming support for clinical project teams, facilitating the development and regulatory approval of products. The ideal candidate will have a strong background in statistical programming, particularly with SAS, and experience in the pharmaceutical industry.

Skills & Requirements

Must-have

  • SAS programming for derived datasets
  • Clinical data structure understanding
  • CDISC standards knowledge
  • Regulatory submission preparation
  • Cross-functional team collaboration

Nice-to-have

  • Drug development process knowledge
  • Global regulatory requirements familiarity
  • Experience with R software
  • Linux operating system experience

Key Requirements

  • Bachelor's degree in statistics, biostatistics, mathematics, computer science or life sciences
  • Demonstrated experience of programming in industry
  • Proficiency in SAS
  • Understanding of clinical data structure (e.g. CDISC standards)
  • Skills in MS office, XML, Pinnacle 21
  • Ability in handling and processing upstream data
  • Ability in providing outputs to meet downstream requirements
  • Understanding of regulatory, industry, and technology standards
  • Knowledge of statistical terminology, clinical tests, medical terminology and protocol designs
  • Ability to work in a team environment

Work Rights

Not specified

Tailored Resume

Cover Letter