Toxicologist/Project Coordinator, Health Consulting
Greater Seattle Area
Toxicologist/Project Coordinator, Health Consulting
Greater Seattle Area
Project coordinator with a background in molecular toxicology and water quality research. Experience in health effects evaluations as a result of over six years with a toxicology consulting firm coordinating fast-paced human and environmental toxicology, industrial hygiene, and professional education-related projects. Highly proficient at prioritizing and monitoring the progress of diverse project timelines; reviewing and interpreting scientific data and literature, medical records, and regulatory information; and communicating scientific information to non-technical audiences.
(Privately Held; 11-50 employees; Environmental Services industry)
November 2002 — Present (7 years 2 months)
Project coordinator responsible for monitoring the progress of diverse human and environmental toxicology, industrial hygiene, and health assessment projects. Communicate with clients and laboratories, and act as a liaison between project team members (toxicologists, industrial hygienists, physicians and/or engineers).
(Educational Institution; 1001-5000 employees; Higher Education industry)
January 2002 — October 2002 (10 months)
Optimized a molecular tool for identification and investigation of gene expression changes caused by exposure to waterborne contaminants.
(Primary/Secondary Education industry)
January 2001 — June 2001 (6 months)
(Government Agency; 5001-10,000 employees; Environmental Services industry)
April 1997 — January 1999 (1 year 10 months)
Contributed to the development and validation of a metal protein as a biomarker for assessing metal contamination in freshwater lakes.
Certificate , Clinical Trials , 2007 — 2008
• Course-required completion of consent form documentation and an IRB application for an experimental phase II HIV vaccine clinical trial.
• Familiarity with clinical research-related Code of Federal Regulations, Good Clinical Practices and human subject confidentiality policies.
• Knowledge of the stages of clinical trials, including study initiation, site management, data management and study close-out.
MS , Molecular Toxicology , 1999 — 2001
BS , Environmental Biology , 1991 — 1996