Director of Biostatistics page is loaded
Director of Biostatistics
Apply locations Princeton NJ US, Cambridge MA US, Boudry, Seattle WA
Time type: Full time
Posted on: Posted 3 Days Ago
Job requisition id: R1589073
Working with Us Challenging. Meaningful. Life changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working with us.
At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science. In oncology, hematology, cell therapy, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
Position Summary
The Director of Biostatistics is a member of a cross functional team and contributes to the development of compounds within a therapeutic area. Drives the design of innovative and efficient clinical trials, including the selection of populations to study and endpoints to use. Develops trial designs that address study objectives that will support regulatory approval and market access. Contributes to Clinical Development Plans, submissions, and post submission strategies, preparations, and defenses. Provides guidance and management to statisticians to ensure high quality and timely deliverables. Manages resources, sets priorities, and ensures consistency and adherence to standards therein.
This position requires on site attendance in Princeton, New Jersey
Key Responsibilities
1. Drives innovative and efficient study design. Develops study designs that address study objectives that will support regulatory approval, medical research and market access.
2. Independently leads, initiates, and oversees the statistical support for the development of compounds within a therapeutic area.
3. Provides guidance and management to statisticians to ensure high quality and timely deliverables.
4. Effectively engages as a matrix team m