Lisa has been at Bristol-Myers Squibb for 15 years. Her first 10 + years was spent in Clinical Pharmacology where she ran clinical pharmacology studies and provided support for oncology and metabolic drug development. For 4 years, Lisa has been a Documentation Lead supporting Clinical Pharmacology aspects of worldwide oncology submissions. For the last year Lisa transitioned into the Global Regulatory Strategy group where she is supporting the development of oncology compounds.