Elizabeth Rivera is a Associate Director and Program Manager, Global Clinical Data Standards at Merck. She possess expertise in in vivo, dmpk, drug discovery, pharmacology, drug metabolism and 2 more skills. Colleagues describe her as "I worked with Betsy for approximately 2 years in a Discovery DMPK setting. Betsy is a knowledgeable pharmacokineticist with considerable experience in animal handling and animal models. She also has an extensive understanding of the operational aspects of the preparation and conduct of, and the outsourcing of preclinical studies. She has a interest in understanding other roles within the pharmaceutical industry and is always enthusiastic about learning new skills. Betsy is an organized, efficient and motivated scientist, is very easy to work with, and is a supportive colleague and a great team player. " and " Runs effective meetings with ease! I had the pleasure of working with Betsy in both lab-based and project-management settings. In both settings, I was impressed with Betsy’s organizational and time management skills while juggling multiple priorities simultaneously. Betsy is extremely efficient and someone who it is a pleasure to work with. Importantly, Betsy can take control of a meeting with highly engaged scientists and rein in the conversation when it gets off topic. Betsy would be a great addition to any team."