Manager, Statistical Programming

Bristol Myers Squibb UK

Uxbridge, United Kingdom
On-site
Sas programming for derived datasets
Cdisc standards understanding
Clinical data handling and processing
Bristol Myers Squibb is seeking a Manager of Statistical Programming in Uxbridge, UK, to provide programming expertise for clinical project teams. The ideal candidate will have a strong background in statistical programming, particularly using SAS, and will play a pivotal role in supporting the development and regulatory approval of BMS products

Job Summary

  • 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.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager of Statistical Programming in Uxbridge, UK, to provide programming expertise for clinical project teams. The ideal candidate will have a strong background in statistical programming, particularly using SAS, and will play a pivotal role in supporting the development and regulatory approval of BMS products.

Skills & Requirements

Must-have

  • SAS programming for derived datasets
  • CDISC standards understanding
  • Clinical data handling and processing
  • Regulatory submission preparation

Nice-to-have

  • Collaboration with cross-functional teams
  • Continuous improvement initiatives
  • Adaptability to new technologies

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 and relational database
  • Skills in MS office, XML, Pinnacle 21
  • Experience with upstream data handling (e.g., multiple data forms, workflow, eDC, SDTM)
  • Experience with downstream outputs (e.g., ADaM, Data Definition Table, e-submission)
  • 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

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