
BioCryst Pharmaceuticals
Birmingham, AL Office
2190 Parkway Lake Drive
Birmingham, Alabama 35244
Phone (205) 444-4600
Fax (205) 444-4640
Cary, NC Office
2425 Kildaire Farm Road
Stuite 106
Cary, North Carolina 27518
Phone (919) 859-1302
Fax (919) 851-1416
Jon Stonehouse, a pharmaceutical executive for more than 20 years, has strong commercialization, financial transaction, business development and management expertise. He most recently served as Senior Vice President of Corporate Development at Merck KGaA with responsibility for global licensing and business development, corporate mergers and acquisitions, corporate strategic planning and alliance management. Among his accomplishments, he was responsible for leading the effort to develop a strategy for Merck that significantly changed the company over the last four years. This culminated with the acquisition of Serono, S.A., the largest biotechnology company in Europe at the time of the agreement.
Stuart Grant joined the Senior Management Team at BioCryst in August of 2007. His recent experience with an established multi-national biotechnology company, coupled with his financial experience, add significantly to the depth of the BioCryst team. Prior to joining BioCryst, Mr. Grant was Chief Financial Officer at The Serono Group, based in Geneva, Switzerland. Operating as part of the leadership team, he was responsible for leading the Finance, Information Technology, and Communications functions, as well as driving the growth of profitability throughout the company. He was extensively involved in communicating strategy and tactics to the investor community. He has held a variety of Senior Operating and Financial positions in Europe and in the United States, and his drive and leadership skills will support the development of BioCryst in the next stages of the Company’s development.
David McCullough joined BioCryst in April, 2007. Prior to joining BioCryst Mr. McCullough served as Director, Global Corporate Development in the Ethical Pharmaceuticals Division at Merck KGaA in Darmstadt, Germany. In that position he was responsible for leading the company's efforts in evaluating the commercial value of specific product opportunities and in the case of the Serono SA acquisition, their entire company portfolio. Mr. McCullough led the commercial assessment of strategic and financial attractiveness of over 40 companies in oncology and other therapeutic areas. Prior to that position, Mr. McCullough was an integral part of the Business Operations and Market Research Team in the Oncology Business Unit of Eli Lilly and Company.
Mr. McCullough received his Bachelor of Science degree from Western Illinois University.
Dr. Babu directs a team of crystallographers and oversees the drug design and computer modeling efforts of the company. Having joined the Company in 1988, Dr. Babu was BioCryst's first full-time employee. Prior to joining BioCryst, he served five years on the biochemistry faculty at the University of Alabama at Birmingham.
Dr. Walter Gowan joined BioCryst in September 2006. Dr. Gowan has more than 20 years of experience in managing pharmaceutical product development programs. His experience includes many dosage forms including oral solutions, oral suspensions, tablets, capsules and sterile products (IV, IM and SC). Dr. Gowan has experience in all stages of product development including formulation development, process development, clinical supplies manufacturing, scale up, process validation, technology transfer, and the resolution of manufacturing issues. Many of his projects have resulted in US and European regulatory filings as well as several products. Prior to joining BioCryst, Dr. Gowan held the position of Senior Director Pharmaceutical Sciences at Cubist Pharmaceuticals where he was responsible for managing the internal and external pharmaceutical product development programs. Prior to joining Cubist, Dr. Gowan held the position of Director Product Development at Solvay Pharmaceuticals where he supervised two product development groups and managed the internal and external development of product candidates. Dr. Gowan received his Ph.D. in Pharmaceutics, B.S. in Pharmacy and B.S. in Biology from the University of Texas.
Ms. Alane P. Barnes joined BioCryst in 2006. Prior to joining BioCryst, Ms. Barnes served as Senior Licensing Associate at the University of Alabama at Birmingham. From 1997, she was responsible for market and competitive analysis to determine intellectual property protection strategy, structuring and negotiation of strategic partnerships and collaborations, technology transfers, licenses and spin-out transactions including engagements for private financing. Ms. Barnes also served as a representative of UABRF and UAB at international biotech meetings and economic development meetings. From 1997 to 2003 Ms. Barnes practiced in a law firm and advised numerous companies on a broad range of issues including general corporate law, regulatory compliance, intellectual property, merger and acquisitions and shareholder agreements, health care law. Ms. Barnes graduated magna cum laude from Cumberland School of Law in 1997 and is a member of Curia Honoris. Ms. Barnes received both her B.S in Natural Science and a minor in Chemistry from the University of Alabama at Birmingham.
Dr. Elliott Berger joined BioCryst in August 2007. Dr. Berger has more than 30 years of experience in the pharmaceutical industry, including over 25 years devoted to management of regulatory affairs supporting new drug and biologic development. Prior to joining BioCryst, he was Vice President, Regulatory Affairs and Quality Assurance, Head of Global Regulatory Strategy at EMD Pharmaceuticals, the North American subsidiary of Merck KGaA. As part of the EMD start-up team, Dr. Berger built and managed the EMD Regulatory Affairs, Clinical Quality Assurance and Drug Safety Groups, as well as the Global Regulatory Strategy Group. At EMD, Dr. Berger submitted and managed over 10 Investigational New Drug Applications in areas of oncology, diabetes, cardiovascular disease, and neurology. Dr. Berger also prepared and submitted the NDA for Cyanokit® which was approved within 6 months of submission to the FDA. Prior to EMD, Dr. Berger was a member of the Senior Executive Team at Astra Pharmaceuticals, most recently serving as Vice President, Regulatory Affairs.
Dr. Berger received both his Ph.D. and M.S. degrees in Biometrics as well as his B.A. degree in Mathematics from Temple University.
Dr. William Sheridan joined BioCryst in July 2008. Dr. Sheridan is a seasoned biotechnology professional, most recently serving as Vice President of North American Medical Affairs at Amgen, Inc. During his 15-year tenure at Amgen, Dr. Sheridan organized and led the company's US Medical Affairs function, making significant contributions to the successful launch of many compounds, including Aranesp®, Enbrel®, Kineret®, Neulasta® and Sensipar®. In addition to his most recent position, Dr. Sheridan held titles at the Vice President level at Amgen in International Medical Affairs, Global Health Economics and Outcomes Research, US Medical Affairs, and Product Development. He played an integral role in building Amgen's international medical affairs function and in forming the health economics and outcomes unit. Dr. Sheridan earned his MB BS degree (M.D. equivalent) at the University of Melbourne in Victoria. Dr. Sheridan is a board-certified fellow of the Royal Australasian College of Physicians (FRACP), with a sub-specialty in medical oncology.
Mr. Robert Stoner joined BioCryst in January 2008. Mr. Stoner brings more than 25 years of progressive Human Resources experience to BioCryst, having worked in a diverse group of industries during his career. Prior to joining BioCryst, Mr. Stoner served as Senior Vice President Human Resources at Smith Breeden Associates, Inc. an institutional financial management company in Chapel Hill, North Carolina. Prior to joining Smith Breeden Associates, Mr. Stoner held the position of Vice President Human Resources at EMD Pharmaceuticals, the North American subsidiary of Merck KGaA. At EMD, Mr. Stoner was responsible for all human resource functions for multiple locations and was a member of the Global HR Team, coordinating and directing global HR initiatives within North America.
Mr. Stoner participated in and graduated from the Merck University Executive Management Program, attending Northwestern University, Kellogg School of Management, Hong Kong University of Science and Technology and INSEAD in Paris. Mr. Stoner received his B.S. in Business Administration from Southern Illinois University.