CAREER HISTORY

February 2006 present
Principal Consultant and Owner, Non-Clinical Safety Assessment, Mountain View, CA

August 2006 February 2009
Vice President, Preclinical Development, Alexza Pharmaceuticals, Inc., Palo Alto, CA

January 2005 - August 2006
Senior Director, Toxicology and Pharmacokinetics, Preclinical and Clinical Development Sciences, Protein Design Labs, Fremont, CA

April 2003 - January 2005
Vice President, Non-Clinical Research and Development, DURECT Corporation, Cupertino, CA

April 2000 - March 2003
Executive Director, Drug Safety and Evaluation, Non-Clinical Research and Development, DURECT Corporation

April 1996 - April 2000
Department Head, Toxicology, Roche Bioscience, Urology and CNS Division, Palo Alto, CA

July 1995 - March 1996
Principal Research Scientist, Toxicology, Roche Bioscience, Neurobiology Preclinical Research, Palo Alto, CA

October 1992 - June 1995
Toxicologist II, Syntex Preclinical Research and Development,
Palo Alto, CA

September 1990 - September 1992
Toxicologist I, Syntex Preclinical Research and Development, Palo Alto, CA

NonClinical Safety Assessment
Michael Taylor , Ph.D., DABT
650-796-2683
 micjtay@gmail.com

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