Robert Neville has served as Savara’s CEO and Chairman since he co-founded the company in June 2008. From January 2003 to December 2004, he served as managing director of Clockwise Consulting, where he worked with the Texas Children’s Hospital and the Baylor College of Medicine to develop an ICU-based monitoring and diagnostic device. From June 2000 to December 2002, he served as Vice President of Engineering at BMC Software where he oversaw the integration and expansion of the product line based on the acquisition of his previous company. From June 1998 to May 2000, Mr. Neville served as co-founder and CEO of Evity, Inc. where he led the development of the company until its acquisition by BMC Software. Based on his work at Savara and Evity, Mr. Neville was honored as a two-time finalist for the Ernst & Young Entrepreneur of the Year award. Mr. Neville holds a post-graduate Engineering degree from the University of Natal South Africa.
Dr. Taneli Jouhikainen is a co-founder of Savara, has served as Chief Operating Officer since October 2009. From October 2006 until September 2009, he served at Akela Pharma Inc., a public clinical stage specialty pharmaceutical company focused on orphan drugs and inhalation products, first as Head of Corporate Development, and subsequently as interim CEO until the company’s merger with Nventa Biopharmaceuticals. From January 2004 to September 2006 he served as President of LAB Pharma Oy, and Head of the Drug Development Business Unit of its parent company, at LAB International, Inc., a public clinical stage specialty pharmaceutical company. From January 2001 to January 2004 he served at Focus Inhalation Oy, a clinical stage specialty pharmaceutical company focusing on inhaled products, first as Vice President of Business Development & Strategy, and subsequently as President & CEO, until the merger of Focus Inhalation with LAB International, Inc. From May 1994 to December 2000, he served at Schering AG, a global pharmaceutical company, first as Research Manager, and subsequently as Head of Clinical Development. Dr. Jouhikainen holds an MD degree, and a Ph.D. degree in hematology and immunology from the University of Helsinki, and an MBA from the Helsinki School of Economics.
Ms. Cecilia Ganslandt (MD, MSc Pharmaceutical Medicine) serves as Head of Medical Affairs and has more than 19 years of experience from positions within global clinical development and medical affairs in small, mid-size and large pharma companies. She has supported a number of clinical development programs from early clinical phase up to and beyond marketing authorizations in Europe, US and Asia. Prior to joining Savara, she was CMO for Serendex Pharmaceuticals, assuming overall responsibility for nonclinical and clinical development.
David Lowrance has served as Savara’s Chief Financial Officer since November 2016. From September 2014 to October 2016, Mr. Lowrance served as the Chief Financial Officer and Treasurer of Edgemont Pharmaceuticals, a fully-integrated specialty pharmaceutical company with multiple marketed products in the CNS space. From April 2011 to September 2014, Mr. Lowrance served as the Chief Financial Officer and Secretary of Acucela Inc., a clinical-stage biotechnology company that specializes in ophthalmic therapeutics, where he was responsible for overseeing all aspects of Acucela’s day-to-day operations, business development and growth endeavors, investor relations and corporate communications. While at Acucela, Mr. Lowrance helped lead a $162 million international IPO, with a listing on the Tokyo Stock Exchange. From March 2003 to April 2011, Mr. Lowrance was Vice President and Chief Financial Officer of Cumberland Pharmaceuticals Inc., a specialty pharmaceutical company focused on commercializing branded prescription products, where he oversaw all aspects of finance and accounting, business and growth strategy and product development. Mr. Lowrance, a CPA, holds a B.B.A. in Accounting from the University of Georgia.
Dr. Lord (PhD) serves as Head of Pharmaceutical Development and is responsible for all CMC activities. He has over 22 years of inhalation product development experience including leadership roles at pharmaceutical companies like Rhône-Poulenc Rorer and Nektar Therapeutics. He has experience across multiple inhalation formulation and device technologies including dry-powder inhalers, pressurized metered dose inhalers and nebulizers.
Mr. Marich (MBA) is one of the founders of Savara and serves as Head of Business Operations. He has significant experience managing the financial and logistical components of large multi-team projects across numerous industries including enterprise software and pharmaceutical product development. Mr. Marich has co-founded numerous companies from inception to exit and specializes in business strategy, corporate structures, fundraising, and project management.
Dr. Tarnow serves as Head of Nonclinical Development and has more than 15 years of experience from biotech and mid-size pharma companies and from academia. She has experience in managing bioanalytical programs, clinical development projects from early phase to Phase III and extensive laboratory research experience. Dr. Tarnow is Doctor of Veterinary Medicine and holds a PhD in pathophysiology from University of Copenhagen. Her latest position in academia was Professor of Veterinary Clinical Pathology and prior to joining Savara, she served as Medical Manager in Serendex.
Ms. Vinge serves as Head of Regulatory Affairs and is responsible for all regulatory activities. She has more than 14 years of experience in regulatory affairs focusing on biopharmaceutical products within rare diseases. She has successfully driven the regulatory development strategy and registration activities for several projects at pharmaceutical companies like Pfizer, Takeda and Serendex. Ms. Vinge holds a Master of Pharmaceutical Science from University of Copenhagen and a Diploma of Pharmaceutical Regulatory Affairs.
Dr. Lawson serves as Senior Director of Quality at Savara and has more than 20 years of experience serving regulated industries in engineering, project management, process validation, regulatory and quality operations capacities. Dr. Lawson is responsible for the oversight of Clinical Quality and GMP Manufacturing Operations including batch release, quality investigations, validation, quality training, and management of internal/external inspections. Dr. Lawson holds a B.S. in Chemistry from Tarleton State University and a Ph.D. in Chemical Engineering from Columbia.