Manager, Sdtm Statistical Programming

Bristol Myers Squibb

Warsaw, Poland
Base: zł209,290 - zł253,607; bonus/equity: + incen...
Hybrid (50% onsite)
Sas programming for sdtm datasets
Cdisc standards expertise
Regulatory submission experience
Bristol Myers Squibb is seeking a Manager for their SDTM Statistical Programming team in Warsaw, Poland, to oversee the implementation of SDTM standards and ensure the quality of statistical programming deliverables for regulatory submissions. The ideal candidate will have a strong background in clinical/statistical programming and experience with CDISC/SDTM standards

Job Summary

  • This role is responsible for driving excellence and consistency in the SDTM implementation team to support regulatory submissions.
  • The position requires overseeing the creation and validation of eCRT packages while ensuring adherence to CDISC standards.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs to support employee goals both at work and in personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager for their SDTM Statistical Programming team in Warsaw, Poland, to oversee the implementation of SDTM standards and ensure the quality of statistical programming deliverables for regulatory submissions. The ideal candidate will have a strong background in clinical/statistical programming and experience with CDISC/SDTM standards.

Salary

Base: zł209,290 - zł253,607; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs provided

Skills & Requirements

Must-have

  • SAS programming for SDTM datasets
  • CDISC standards expertise
  • Regulatory submission experience
  • Protocol and synopsis review
  • CRF annotation and metadata

Nice-to-have

  • Knowledge of AI in SDTM deliverables
  • Experience with BMS automation tools
  • CRO vendor management skills
  • Pinnacle21 validation proficiency
  • Global therapeutic area CRF development

Key Requirements

  • Minimum 4 years clinical/statistical programming experience
  • BA/BS in a relevant scientific discipline
  • Expertise in CDSIC/SDTM for regulatory submissions

Work Rights

Not specified

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