Senior Statistician II
Core
Design, delivery, and interpretation of statistical analyses for preclinical and clinical studies, regulatory submissions, and commercialization in the pharmaceutical industry.
Role type
Senior individual contributor statistician
Builds
Statistical analysis plans, study reports, regulatory submissions, and decision criteria for clinical programs
Domain
Pharmaceutical industry, clinical research, regulatory affairs
Required skills
Statistical programming (SAS, R), study design, complex data analysis, regulatory knowledge, statistical modeling and simulation, technical writing, mentoring
Preferred skills
Novel statistical approach development, process improvement, external scientific collaboration
Technologies
SAS, R
Responsibilities
Provide statistical expertise for complex design and interpretation of preclinical or clinical programmes; Develop statistical analysis plans for complex studies; Act as a coach/guide for less experienced statisticians; Contribute to regulatory submissions; Identify opportunities to improve methodology and study design; Communicate research results internally and externally through conferences and publications
Seniority
Senior, hands-on IC