LINDA LUM, Senior Director, Global Scientific & Regulatory Documentation, Bristol-Myers Squibb

Linda Lum, PharmD MBA RPh, is a Senior Director in Global Scientific and Regulatory Documentation at Bristol-Myers Squibb (BMS) Company in Princeton, NJ with 25 years of pharmaceutical industry experience. She serves as lead of the scientific writers for the investigator’s brochures, safety aggregate reports, and risk management documents in the Regulatory department.

As project leader for multiple continuous improvement projects, she enjoys developing and implementing innovative processes to create efficiencies while meeting the changes in regulatory requirements. Linda served as a preceptor for the BMS collaboration in the Rutgers Pharmaceutical Industry Fellowship Program.