Principal Scientist
Current• Provides direct oversight and interacts with the external Contract Research Organizations (CROs) responsible for conducting the quantitative analysis of biological samples in support of small molecule clinical and/or preclinical development. • Develops and implements Standard Operating Procedures (SOPs) for managing GCP and GLP bioanalytical projects conducted by external CRO(s).• Represent the bioanalysis function on the development program teams and present results, timelines, etc. at project team meetings.• Responsible for the scientific quality of the bioanalytical projects in support of clinical and/or preclinical development.• Defines, coordinates, manage and oversees the bioanalytical project timeline. • Collaborate with clinical / preclinical drug development program teams.• Lead bioanalytical method development and validation team for new compounds entering development stage.