The Senior Director of Biostatistics acts as statistical lead with accountability for Ultragenyx product and study deliverables. They will provide strategic input and statistical expertise in advancing clinical programs. They will provide statistical leadership for regulatory submissions and lead implementation of strategies for the Biostatistics and Epidemiology group.

As a Research Scientist, you will collaborate on health economic and health policy research projects, conduct statistical analysis, and contribute to the interpretation of results. Your day-to-day activities may include designing cost-effectiveness and budget impact models, programming health economic models in Microsoft Excel, and communicating research projects to internal teams and external clients.

In this role, you will design, implement, interpret, report and publish the results of retrospective and prospective observational research studies that demonstrates the utility of real-world data (RWD) for life sciences and health system customers. You will also contribute to developing N-Power Medicine’s real-world evidence generation platform.

Contribute to and lead projects that leverage our real-world mental health database and advanced analytics to generate real-world evidence (RWE) in psychiatry. Assist with the design and conduct of studies using real-world data (RWD) that evaluate clinical effectiveness of interventions and effect of different exposures in psychiatry. Work closely with the study team to define research questions and clear deliverables.

The Scientist TMED will use genomic data to advance healthcare by initiating, directing, and executing pre-clinical scientific research and development strategies for oncology and early cancer detection business units. They will plan and execute clinical research and data analysis and communicate results, transforming product requirements into technical specifications.

The Associate Director, Biostatistics will participate in all biostatistics activities in a clinical development program from clinical design to regulatory submission. Includes clinical trial design, statistical analysis development, carrying out modeling and simulation, and overseeing statistical deliverables.

This is an exciting opportunity to lead the Biostatistics efforts supporting Natera’s product portfolio of cutting-edge molecular diagnostic tests. As Lead Biostatistician, you will oversee the design, analysis, and reporting of validation experiments to support our oncology portfolio. The ideal candidate will possess strong communication skills and a deep understanding of biostatistics in analytical validation.