Principal Statistical Programmer
Core
Develop and implement statistical analysis plans and produce QC'd data packages (tables, figures, listings) for clinical trial publications and ad-hoc analysis.
Role type
Principal Statistical Programmer
Builds
Statistical data outputs for Medical Affairs publications and presentations
Domain
Clinical trials / Biostatistics / Pharmaceutical R&D
Required skills
SAS programming, SDTM, ADaM, CDISC standards, post-hoc statistical analysis, macro development, SOP compliance
Preferred skills
Mentorship, advanced programming methods, clinical data environment expertise
Responsibilities
Design, develop, test, and document statistical programming in high-level software packages; Conduct post-hoc statistical analyses of clinical trial data; Produce well-documented data packages including tables, listings, and figures; Collaborate with biostatisticians to develop QC plans and timelines; Coach and mentor new team members.
Seniority
Principal, hands-on IC with mentorship responsibilities