Director
Tina has more than 12 years of experience with clinical trials as both a consultant and permanent employee of Roche Molecular Systems, BioMedicines, Bayer Diagnostics, Chiron and most recently, Vermillion. Her clinical trial management experience builds on another six years of experience researching and developing products, primarily within the diagnostic field.
Tina has been involved in numerous successful clinical trials spanning the US, Canada, EU, and ROW (rest of world). She has worked with companies designing Analytical Studies, Studies for 510(k) Submissions, Studies for Pre-Market Application Submissions, and Post Marketing Studies.
Tina holds a BA in Chemistry from Arizona State University and received her Certification of Clinical Research Associates (CCRA) in 2001.
