Global Regulatory Content Strategy Lead

Bristol-Myers Squibb is seeking a Director for Global Scientific and Regulatory Documentation in Bogotá. This role involves leading a team of scientific writers, mentoring them, and optimizing documentation processes that support the BMS pipeline.

The ideal candidate should have a PharmD/PhD/MD or equivalent with at least 10 years of experience in regulatory documentation. Strong leadership and collaboration skills are essential, as well as a passion for transforming patient lives through science.