In support of IChem Indy, I perform tasks related to the Project Management process by coordinating activities for routine studies in compliance with appropriate protocol, Standard Operating Procedures and regulatory agency guidelines, in a timely, efficient, and quality manner.

Robin works closely with a team of scientists to conduct early phase and registration toxicology and pharmacology studies for the development of pharmaceuticals. Tailors client requirements into protocol development and manages internal and external customer needs to conduct quality studies for lead optimization and registration efforts.

Highlights of Robin’s experience include:*Study Director/Monitor: Designed, conducted, reported and summarized GLP Environmental (E Fate) studies internally and monitored, reported and summarized studies conducted at contract facilities.*Implemented Laboratory Information Management System: Collaborated with vendor, computer validation experts and working group to design, test, validate and implement Debra LIMS.*Standardized Report and Summary Templates: Facilitated the generation of report and summary templates, standardizing formatting and creating boilerplate text for uniform processes; Templates were considered “living” documents and required periodic updates as processes underwent changes and technologies improved*OECD and US EPA Kinetics Determinations: Knowledgeable in both OECD and US EPA degradation rate kinetics determination for best-fit and modeling endpoints.*Principal Investigator of 14C Radioactive Use: Served as Authorized User of 14C Radioactivity for 25 years and Principal Investigator (PI) for 17 years. Responsible for safety communication to working group and management of inventory; completed training for all new Authorized Users.