Manager, Sdtm Statistical Programming

Bristol Myers Squibb

Warsaw, Poland
Base: zł209,290 - zł253,607; bonus/equity: + incen...
50% onsite
Sas programming expertise
Cdisc sdtm standards knowledge
Regulatory submission experience
The role provides expertise to drive excellence and consistency in the SDTM implementation team for regulatory submissions

Job Summary

  • The role provides expertise to drive excellence and consistency in the SDTM implementation team for regulatory submissions.
  • Candidates will oversee CRO vendor activities and ensure adherence to CDISC standards while managing study timelines.
  • Bristol Myers Squibb offers a hybrid work model with competitive benefits and opportunities for career growth in life-changing science.

Matching Summary

The role provides expertise to drive excellence and consistency in the SDTM implementation team for regulatory submissions.

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 expertise
  • CDISC SDTM standards knowledge
  • Regulatory submission experience
  • Clinical trial data integration
  • Pinnacle21 validation tools

Nice-to-have

  • AI automation in SDTM deliverables
  • BMS specific automation tools
  • Cross-functional stakeholder collaboration
  • 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

Tailored Resume

Cover Letter