Research Associate & Supervisor offering 20 + years of experience within a Pharmaceutical (Eli Lilly & Co) and Contract (Covance) Research Laboratories. Working under Good Laboratory Practices (GLP), Food and Drug Administration (FDA), and Drug Enforcement Administration (DEA) regulated environments. Supporting drug discovery research in Toxicology & Early development which includes Environmental Tox, Pharmacology -Cardiovascular, Oncology, Metabolic Disease, Renal, & Neuroscience groups. I have led a Formulation discovery team and Early Development Oncology in-vivo team that have supported multiple compounds which have succeeded in clinical development. For the past 9 years, I have worked in the contract research arena providing Formulations support for ADME, Discovery, Pharmacology, Imaging, Toxicology, and DART studies for global pharmaceutical clients. Specialties: Supervisor, Formulations, Large and small animal study conduct, Discovery, Pharmacology, report writing, team building and management trained, process excellence.