Job Description
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.
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