New Associate Director, Biostatistics

Reporting to the Executive Director, Biostatistics, this position is responsible for collaborating with both internal and external stakeholders to deliver the execution of our Biostatistics strategy. The individual in this position will have the unique opportunity to participate in the rapid growth of a biotech startup. Key Responsibilities: Provide statistical inputs into protocol and clinical study report development, statistical analysis plans, interpretation of statistical analysis results, randomization plans. Provide oversight and review of statistical documents for multiple clinical trials, including TLF shells, eCRFs, specifications of variable derivations, and all deliverables from outside vendors or internal programmers. Develop effective collaborations with others within clinical teams and partner lines (such as Statistical Programming, Data Management, Medical, Clinical Operations, and Regulatory). Ensure that all study level statistical activities are conducted in compliance with relevant regulatory requirements and Immunovant standards. Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports. Oversight statistics and programming vendors. Open to opportunities to utilize innovative statistical methodology to streamline the clinical development process and facilitate optimal decision-making.