This role provides expertise to drive excellence and consistency in statistical programming SDTM implementation within a life-changing pharmaceutical environment
Job Summary
This role provides expertise to drive excellence and consistency in statistical programming SDTM implementation within a life-changing pharmaceutical environment.
The position is primarily responsible for the quality and timely delivery of SDTM artifacts required for downstream activities and regulatory submissions.
Bristol Myers Squibb offers competitive benefits, services, and programs that provide employees with resources to pursue goals both at work and in personal lives.
Matching Summary
This role provides expertise to drive excellence and consistency in statistical programming SDTM implementation within a life-changing pharmaceutical environment.
Salary
Base: zł209,290 - zł253,607; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs
Skills & Requirements
Must-have
SAS programming for SDTM datasets
CDISC standards expertise
Regulatory submission experience
CRO vendor management oversight
Pinnacle21 validation tools
Nice-to-have
AI automation in SDTM deliverables
Deep standards education skills
Hands-on implementation support
Cross-functional stakeholder collaboration
Key Requirements
Minimum 4 years clinical/statistical programming experience