Adrian W. Bott, Ph.D.
Adrian joined the BASi® bioanalysis group in 2006. After 1 year as an analyst, he moved to project management, and has been responsible for multiple method development, method validation, and sample analysis projects, both pre-clinical and clinical. He received a B.A. in Natural Sciences (1986) and a Ph.D. in Chemistry (1989) from the University of Cambridge (UK). Prior to joining the bioanalysis group, he worked for the BASi® electrochemistry group for 15 years following a post-doctoral appointment at Purdue University.
Orlando Bravo , Ph.D.
Orlando joined BASi® in April 2005. He received a PhD. in Organic Chemistry from Texas A&M University and a BS from University of Costa Rica. In his nearly 10 years of experience at BASi® he has extensively worked with method development, method validation, clinical and non-clinical bioanalysis. He has ample experience with LC-MS/MS, UPLC-CAD and LC-fluorescence methods. He has been involved with numerous client audits and inspections. Orlando has also been involved with FDA inspections.
Robert Clegg, B.S.
Robert joined BASi in 2011 after receiving a B.S. in Chemistry (ACS accredited) degree from Purdue University. He spent four years as an analyst with both the bioanalytical analysis and method development/method validation teams before transitioning into a project management role. Robert’s responsibilities include the development and validation of bioanalytical assays, client communications, maintaining deadlines, and issuing reports.
R. Tyler Degraw , Ph.D.
Scientific Team Manager
Tyler joined BASi® in 2006. Previously Dr. DeGraw worked for the Pharmaceutical Division of 3M as a Senior Biochemical Pharmacologist. He received his Bachelor of Science in Chemistry degree from Utah State University and aPh.D. in Pharmaceutical Sciences from the University of Kentucky. Dr. DeGraw originally joined BASi® to work with the BASi Culex ® automated blood sampling system, and served as the principal investigator for an NIH grant to transfer the BASi Culex ® technology to large animals. Tyler is currently a Scientific Team Manager for the Bioanalytical department where his current responsibilities include coordinating, organizing and scheduling projects with personnel and instrumentation. He also continues to work directly with clients in pharmacokinetic analysis and as a principal investigator on bioanalytical projects. He is a member of the American Association of Pharmaceutical Scientists
Scott joined BASi® in 1988 after earning the ACS Certified B.S. in Chemistry from Purdue University. He has extensive experience in instrumental bioanalysis encompassing HPLC with electrochemical and mass spectrometry methods of detection. His areas of expertise include the development and troubleshooting of analytical methods for pharmaceuticals in numerous matrices and implementation of those methods for rapid, high throughput sample analysis. Current responsibilities include clinical and non-clinical bioanalytical sample analysis project management, sponsor communication, data management and report preparation.
Hasantha Jayaratna, Ph.D.
Hasantha first joined BASi® in 1993 as a post-doctoral scientist in electrochemical division where he conducted governmental grant supported research geared towards instrument development for mass screening of children for blood lead contamination. He later joined as a senior scientist in Method Development division of BASi® CRO in 2005. Hasantha has developed and validated numerous bioanalytical LC/MS methods since then and continues with an extensive knowledge of various issues with biological sample analysis and project management.
Steven Kaverman, M.S.
Scientific Team Manager
Steven joined BASi in January of 2013. He worked primarily as an analyst in the bioanalytical division working on validations and sample analysis. During his time as an analyst, Steven gained experience with LC-MS/MS, UPLC-CAD, and LC-fluorescence methods. He also worked on several bioequivalence studies in the pharmaceutical analysis department. Steven spent 2.5 years as an analyst before transitioning into a project management role. He received a B.S. in Pharmaceutical Sciences (2007) from Purdue University along with minors in biology and chemistry. He also received a M.S. in Chemical Education (2012) from Purdue University.
Rachel Sun , Ph.D.
Director, Bioanalytical Development
Dr. Rachel Sun joined BASi® in 2002. She has more than 20 years of experience in pharmaceutical industry in drug development and contract service. She has developed hundreds of bioanalytical assays to support pre-clinical and clinical studies of different chemical identities including small molecules, peptides and oligonucleotides. Before joining BASi®, Dr. Sun worked as scientist in Barr Laboratories (now Teva Pharmaceutical) and V.I.Technologies. She received a Ph.D. in Chemistry from New York University and a B.S. in chemistry from Peking University, China. Dr. Sun has numerous presentations at professional meetings, such as AAPS and ASMS..