Transforming clinical data starts with you!

The primary responsibilities of this position are to provide strategic statistical leadership and drive scientific excellence across our clinical development portfolio. This is a high-impact leadership role supporting biotech and pharmaceutical clients from early development through regulatory submissions and approvals.  

The primary responsibilities of this position are to provide statistical consulting to biotech and pharmaceutical clients throughout drug development, with a focus on clinical data analysis strategy, study design, regulatory submissions and communications, mentoring statisticians, and supporting business proposals.  

The primary responsibilities of this position are to provide statistical consulting to clients in the biotech/pharmaceutical industry in their drug development programs with a focus on protocol/study design, analysis planning, and regulatory submission strategies.  

The primary responsibilities of this position are to provide leadership in planning and conducting data analyses in clinical studies, and participate in planning and data analyses for regulatory submission.  

The primary responsibilities of this position are to assist with study level statistical related activities, particularly to write statistical analysis plans, prepare mock tables/figures/listings, and generate statistical analyses for clinical studies conducted by pharmaceutical and biotech companies.