LINICAL ACCELOVANCE AMERICA, INC.
STUART, FLORIDA

in 2009, 2010, and 2011; and received a “Highly Recommended” distinction in 2013.  This external validation of Accelovance’s vaccine research experience and success is a result of our ability to guarantee budgets, control timelines, and accelerate patient enrollment – delivering business solutions that address our clients’ clinical needs. Established in 2005 with a corporate mission to improve the quality and predictability in clinical research, Accelovance has made significant strides in the industry by combining strong business and operational perspective with clinical and medical expertise. Mission and Vision Accelovance's mission is to unite our world-class expertise to advance innovative treatments through clinical development. We accomplish this by Mr. Trevisan is an entrepreneur who has founded four companies, including Accelovance, Inc. in 2005. Prior to Accelovance, Mr. Trevisan founded TherImmune Research Corporation, a Contract Research Organization (CRO) specializing in preclinical and early stage clinical drug development services for the pharmaceutical, biotechnology, and government markets. He also founded CommSys Corporation, a provider of outsourced billing services to the telecommunications industry. In 1987, Mr. Trevisan co-founded his first company, National Clinical Research Centers (NCRC), a CRO specializing in Phase II-IV clinical studies. NCRC deployed a unique method for running clinical trials which was successful in reducing the timeframe in conducting multi-center trials in broad-based indications. Each of Mr. Trevisan's prior companies maintained year-over-year growth and were ultimately acquired by public companies. Jeffrey T.  Rudolph, MBA has 25 years of CRO and pharma/biotech industry experience including extensive global CRO team leadership experience. Jeff is a seasoned planner and CRO business executive who knows how to deliver results in a "scale up" environment. During his time in the industry, he has worked with clients ranging from small biotech to large pharma, providing solutions that address their specific needs. In his role as vice president, Global Business Development at Chiltern, Jeff was responsible for managing the global biotech sales team in North America, Europe and Asia Pacific. Prior to Chiltern, Jeff spent four years as one of five regional business development Executive Directors for ICON, and four years each in business development at PRA Health Sciences and SGS Life Sciences. Additionally, Jeff spent four years as Global VP of Sales/Marketing for Healthcare Communications Group, and was employee number five when this organization was a startup (the company eventually sold after significant growth/expansion). His background encompasses extensive professional business experience growing pharma services companies from scratch to $100M/year in revenue. He holds a Master of Business Administration degree from the University of Texas and a B.S. in Biochemistry from the University of Missouri. Dr. Dave leads Accelovance's Medical Affairs & Drug Safety group. Dr. Dave has 25+ years of Phase I-IV clinical research experience including the conduct of over a 100 studies with a focus on hematology, oncology and transplantation as well as other areas of internal medicine. Dr. Dave provides integrated drug development and therapeutic advice, management of clinical trials, and expertise and due diligence for biotech, small, medium and large pharma and VC companies. He has basic science expertise in gene regulation, gene therapy and tumor immunology, clinical and academic expertise in hematology including coagulation disorders, oncology and transplantation, and industry experience in hematology/oncology drug development from pre-clinical to phase IV space and in biosimilars/biobetters and immunotherapeutics. Prior to joining Accelovance, Dr. Dave held positions at Quintiles, George Washington University Medical Center and VA Medical Center in Washington, DC and NIH in Bethesda, MD. Dr. Dave holds a MB, ChB from the University of Sheffield and a MBA from the TRIUM program (jointly awarded by NYU, London School of Economics and HEC). Dr. Oliver serves as our Chief Science Officer, leveraging his strategic, scientific, and industry experience to guide Sponsor product development. Prior to joining the Accelovance team in 2013, Dr. Oliver was the Chief Executive Officer at Phage Pharmaceuticals, Inc. and prior to that was a Principal at Trinity Drug Partners, LLC. Dr. Oliver has amassed significant clinical research experience in both preclinical and clinical experimentation in academia and the pharmaceutical industry. Dr Oliver has strong therapeutic experience in the areas of oncology, hematology, vaccines, nutritional support, cytokines regulation, infectious diseases, immunopharmacology, renal disease, and transplantation. Dr. Oliver has served on the executive management team of both public and private pharmaceutical companies in a Vice President/COO role. He has served on the clinical faculty of Mercer University, Emory University, and the University of North Carolina. He also was a collaborative researcher with the Centers for Disease Control and Prevention, Hospital Infections Division. Dr. Oliver received his Doctor of Pharmacy degree from Mercer University in Atlanta. He has published a number of peer-reviewed articles in the area of immunopharmacology and oncology and is a member of the American Society of Clinical Oncology. Dr. Wendy (Wen-Ying) Wang is the Managing Director at Accelovance China. As Head of Accelovance China, Dr. Wang helps western pharmaceutical companies with global clinical trial registration, import drug registration, regulatory consultancy, clinical site management, and project management of multi-center global clinical trials in China. Dr. Wang has broad experiences in research, technical, sales, quality, medical and regulatory affairs within the biotechnology and pharmaceutical industries in the areas of bioactive enzymes, medicines, and vaccines in Greater China and Asia Pacific regions. Dr. Wang earned her clinical medicine degree from Shandong Weifang Medical College, Master's degree in gastroenterological physiology from Peking Union Medical College, and her PhD in the regulation of angiogenesis by vascular endothelial growth factor from the University of Bristol in the United Kingdom.