Manager, Sdtm Statistical Programming

Bristol Myers Squibb UK

Warsaw, Poland
Base: zł209,290 - zł253,607; bonus/equity: + incen...
50% onsite
Sas programming for sdtm datasets
Cdisc standards expertise
Regulatory submission experience
The role is responsible for providing study SDTM deliverables that support analysis, reporting activities, and regulatory submissions

Job Summary

  • The role is responsible for providing study SDTM deliverables that support analysis, reporting activities, and regulatory submissions.
  • Candidates must oversee CRO/vendor programming activities to ensure adherence to CDISC standards and receive quality timely deliverables.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs to help employees pursue their goals both at work and in personal lives.

Matching Summary

The role is responsible for providing study SDTM deliverables that support analysis, reporting activities, and 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 for SDTM datasets
  • CDISC standards expertise
  • Regulatory submission experience
  • CRO vendor oversight
  • Pinnacle21 validation tools

Nice-to-have

  • AI automation in SDTM deliverables
  • BMS specific automation tools knowledge
  • Global therapeutic area CRF development
  • Structured training leadership
  • Deep standards education capability

Key Requirements

  • Minimum 4 years clinical/statistical programming experience
  • BA/BS in relevant scientific discipline
  • Expertise in CDISC/SDTM standards
  • Experience with SAS Programmer supporting clinical trials

Work Rights

Not specified

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