Principal Statistical Programmer
Core
Lead statistical programming for clinical trials, ensuring data accuracy and compliance for regulatory submissions in oncology, hematology, immunology, and cardiovascular disease.
Role type
Principal Statistical Programmer (hands-on IC with strategic influence)
Builds
Submission-ready clinical data packages and electronic submissions for global health authorities
Domain
Biopharma / Clinical Data Management / Regulatory Affairs
Required skills
SAS programming, CDISC standards (SDTM/ADaM), end-to-end clinical data pipeline management, regulatory submission expertise, cross-functional collaboration, process improvement
Preferred skills
Team leadership and mentorship experience (via careerplan.io/jobs/R1604796-principal-statistical-programmer-at-bristolmyerssquibb)
Technologies
SAS, CDISC, SDTM, ADaM
Responsibilities
Design and implement technical solutions for complex clinical data; review statistical analysis plans; shape programming strategy; advise senior stakeholders on risk and resolution; lead and support electronic submissions; mentor technical professionals
Seniority
Principal, hands-on IC with strategic influence