Date: 02-Jan-2015
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Associate Director, Toxicology
Responsible for safety pharmacology and toxicology study design, dosage selection, study initiation and monitoring, data review, and reporting. This involves management of a significant number of staff (and their processes) at multiple contract facilities (CROs) to ensure that the timing requirements of the internal project teams are achieved.
Act as an internal expert and mentor for Discovery project teams to ensure appropriate evaluation of candidate compounds for further development. Facilitate the transition of lead discovery candidates through the nomination process and into development.
As a participant on global project teams, collaborate with Japanese counterparts to design nonclinical safety studies and overall nonclinical safety strategy.
Author internal documents and regulatory submissions and directly participate in regulatory interactions. As needed, perform literature reviews and data summaries, and deliver internal presentations.
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BioTech FYI Center
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