Global Regulatory Documentation & Content Strategy Director

Bristol-Myers Squibb is seeking a Director for Global Scientific and Regulatory Documentation, focusing on establishing a strong team of scientific writers. The role involves creating and implementing process improvements in documentation, managing resources, and mentoring writers.

The ideal candidate will possess a PharmD/PhD/MD or a bachelor's degree with at least 10 years of experience in regulatory documentation. Key contributions include leading innovation projects and enhancing document quality standards.