When you work with Celerion, you have access to over 100 years of collective hands-on experience from our senior management team. Clients receive the CRO industry knowledge required to move past the competition.
Learn more about any Celerion team member by clicking below.
Dr. Thornton is a life sciences executive with a track record of building and managing businesses through technology transfer, product development and targeted marketing programs. Most recently, she was a cofounder of BioVerum Partners, a healthcare advisory services firm, and served as President and CEO. Prior to that, Dr. Thornton was an Executive in Residence with MDS Capital, a healthcare venture capital firm. Dr. Thornton also held the position of President, Global Clinical Research and Central Labs for MDS. In this position, Dr. Thornton had responsibility for all facets of the business and guided the organization through major change following the acquisition of six regional companies. Prior to MDS, Dr. Thornton was Director of Worldwide Business Development for SmithKline Beecham, now GlaxoSmithKline, where she led teams in the negotiation and acquisition of new products for the pharmaceutical business. She also served as Project Manager, leading multidisciplinary project teams in the development of new biotechnology products. Dr. Thornton has substantial experience in international business development, deal sourcing and due diligence, integration and restructuring, and the achievement of sustained financial growth through the development of new business strategies and operating efficiencies. She earned her PhD in Molecular Biology from the University of Pennsylvania and an M.S. Microbiology and B.S. Psychology from Pennsylvania State University.
Ms. Rosal is a senior financial executive with extensive business management experience in North America and Europe. Most recently, she served as Chief Financial Officer and Vice President of Internal Services for Constructive Technologies Group, an Irvine, California-based consulting and engineering firm. Prior to that, Ms. Rosal was Managing Partner and Chief Financial Officer for BioVerum Partners, a healthcare advisory services firm. Ms. Rosal has also held Vice President Positions in finance and administration, and business systems and processes at MDS. Among her accomplishments, Ms. Rosal led a finance team of 70 professionals worldwide in the consolidation of dispersed operations across 20 countries into a harmonized global business. She has developed integrated financial reporting and budgeting tools to improve operations and profitability and implemented pricing structures to achieve desired margins consistent with business targets. She holds a Bachelor of Arts degree in Business Economics from University of California, Santa Barbara and is also a Certified Public Accountant (“CPA”) with membership in the American Institute of CPAs, and the California Society of CPAs.
As Chief Medical Officer, Dr. Hoffman leads the global medical staff and provides medical oversight and expertise to support early clinical research studies.
Dr. Hoffman has over 28 years of knowledge and experience as a physician in the pharmaceutical, device, and CRO industries to this role. He has extensive experience in global drug development, medical affairs, pharmacovigilance and regulatory affairs, and has a proven track record in building, managing and globalizing medical teams.
Prior to this role, Dr. Hoffman served as Chief Medical Officer at Patient iP, providing clinical leadership around Patient iP’s innovative platform, customer programs and related medical affairs activities. Dr. Hoffman has also held the roles of Chief Medical Officer and Senior Vice President and General Manager over the Biopharmaceutical Business Unit at Theorem Clinical Research, leading the development of drugs and biologics. Previously in his career, he held positions of increasing responsibility in Medical and Scientific Affairs at Baxter, Hospira and Covance, providing senior-level strategic direction for Phase II-IV programs.
As Senior Vice President of Global Clinical Development, Dr. Klaus Fischer leads a global group of clinical development professionals focused on the execution of clinical studies in patients. Very experienced in clinical project management and monitoring, these teams work with clinical sites and alliance partners on a global scale to generate key development data for critical decisions about whether or not to progress new drugs or treatment concepts to the market. These clinical development professionals leverage drug development and regulatory knowledge, bioanalytical expertise, data analysis and medical writing expertise within Celerion to provide complete solutions for clients’ clinical development needs.
Combining advanced training in pharmacy and business administration, Dr. Fischer brings to his role 20 years of experience in new product development, clinical study management, medical marketing and executive leadership with Hoechst, Hoechst-Roussel, Aventis and as the CEO of the Assign Group. In this capacity, Dr. Fischer founded the company in Europe and built the organization into an efficient clinical research operation with a track record in managing regional and global clinical studies. Over the years he and his colleagues have worked on several oncology treatments, vaccines, and other medicines that have progressed into late stage development and the marketplace.
Dr. Fischer has given numerous invited lectures at scientific meetings and academic institutions. He received his scientific degree from Ludwig-Maximilian-University in Munich.
Mr. Bach serves as Vice President of Clinical Research. He is responsible for leading the largest global Phase I and IIa clinical operations networks in the industry, and has extensive experience in private and public clinical research environments, and a thorough understanding of the needs and requirements for clients. Prior to this role, he was recruited into the role of Clinical Site Director for the Phoenix, AZ facility for MDS Pharma Services to rebuild and reposition for growth. Mr. Bach aggressively grew the business, while streamlining operations to deliver high quality service in a timely manner. The successful turnaround of this facility led to the expansion of the clinic from a 120 bed facility to a capacity of over 300 beds. Mr. Bach led the team for the design and build of the new state-of-the-art clinical research facility, successfully launching it on-time and on-budget. Mr. Bach also served as Clinical Operations Manager in Lincoln, NE, where he was responsible for all operational execution, management and conduct of all clinical trials. Mr. Bach began his career with MDS Harris in 1998 where he held positions of increasing responsibility, enabling him to gain hands-on experience of all aspects of the business.
In addition to serving as an executive board member for Arizona State University Research committee, he is also an active member of the Society of Clinical Research Associates, Arizona Bio Industry Association and the Association of Clinical Research Professionals. Mr. Bach holds a B.S. in Biology from the University of Nebraska.
Dr. Combs serves as the Vice President of Data Management and Biometrics, one of the largest and most experienced groups in the industry. In this role she is responsible for modeling and simulation, protocol development, data programming, biostatistics, pharmacokinetics, and medical writing. Dr. Combs has successfully harmonized global processes from legacy companies and sites, to deliver consistency of data and to ensure the highest level of scientific excellence across all client programs.
Dr. Combs has over 20 years’ experience in clinical development and has done extensive research in a variety of areas with publications and presentations on topics focusing in safety, tolerability, pharmacokinetics, and efficacy of new compounds and formulations. Dr Combs has specialized in early clinical research for the past 17 years, allowing her to have an in-depth expertise in the scientific and logistical challenges faced by clients. She is currently focused on the automation of data delivery and innovative study designs including adaptive trials, to accelerate drug development.
Dr. Combs joined MDS Harris in 1997 and held positions of increasing responsibility in biostatistics and pharmacokinetics before leading the Global Clinical Pharmacology Sciences department at MDS Pharma Services.
Previously in her career, Dr. Combs was a member of the research team at the University of Iowa Clinical Trials Data Management Center, where she participated in the planning, analysis, and interpretation of several Phase III clinical trials. Dr. Combs holds Master’s and PhD Degrees in Biostatistics from the University of Iowa, as well as a Bachelor of Science degree in Mathematics and Statistics from the University of Nebraska at Kearney.
As Vice President of Global Drug Development, Dr. Pritchard leads a global team of drug development and regulatory affairs experts, project management professionals and alliance managers that work actively with clients to bring their drug products efficiently through early clinical testing.
Dr. Pritchard brings 30 years of drug development experience to his work, including pre-registration work on five currently marketed pharmaceuticals and several that are currently in clinical development. Leveraging his experience in leading international teams of scientists at large pharmaceutical companies, Dr. Pritchard founded and led a group of consultants and program directors within a full service CRO that collectively worked on nearly 40 integrated drug development programs, bringing several of these through IND into phase I and II clinical trials.
Dr. Pritchard has given numerous invited lectures at scientific meetings and academic institutions and is an author on over 120 scientific publications and abstracts. He is the 2000 Alumni Fellow of the Penn State College of Medicine, and named one of nine “Notable People in Pharmaceutical R&D” by R&D Directions magazine in 2009. He currently serves on the Therapy Acceleration Program Committee for the Leukemia and Lymphoma Society (LLS), the LLS North Carolina Chapter Board of Trustees and the Executive Committee of the Research Triangle Park Drug Metabolism Discussion Group where he has been past Chair and Treasurer.
As Vice President of Global Business Development, Mr. Maya leads the global sales organization. As a business leader at Celerion, Mr. Maya is focused on developing strategies and managing their execution driving top line and P&L growth. Mr. Maya has implemented several key account initiatives to strategically position Celerion as a top CRO service provider in the market. He has focused on strengthening the Business Development team by implementing sales performance standards and metrics, as well as adding top sales talent.
Prior to this role Mr. Maya held the roles Vice President, Business Development for Early Stage Development and Vice President, Business Development for Pharmacology/DMPK at MDS Pharma Services.
Mr. Maya has also held the roles of Vice President, Sales and Marketing at TargetRx and Vice President, General Manager at Dendrite Intl. where he built successful international operations throughout Europe, Latin America and Canada.
Mr. Maya has over 24 years experience in sales and marketing within the life science vertical, 15 of those within the pharmaceutical industry. He has held key leadership sales and marketing positions with Schering Plough, where he launched multiple products and built sales, marketing and operations organizations. Mr. Maya has a proven track record of launching products in oncology, anti-infective, dermatology and cardiovascular therapeutic areas.
Mr. Maya received his B.S. in Education from Brooklyn College, Brooklyn, New York.
As Vice President of Global Bioanalytical Services, Dr. Farmen leads one of the preeminent bioanalytical groups in the industry. In this role he is responsible for the bioanalytical groups in Lincoln, NE USA and Zurich, Switzerland. These groups offer exceptional expertise in both small and large molecule method development and sample processing in an extremely automated and compliant environment.
Dr. Farmen comes to Celerion with over 30 years of experience in the contract research organization (CRO) and pharmaceutical industries. Prior to joining Celerion, he held executive positions at PharmOptima, a CRO that specializes in ocular research services; Eurofins AvTech Laboratories, a CRO that specializes in small and large molecule bioanalytical chemistry as well as QC testing and analysis of finished drug products and pharmaceutical ingredients; and Camargo Pharmaceutical Services, a CRO that provides scientific and regulatory oversight during the drug development process. Dr. Farmen also held leadership positions in the bioanalytical sciences at MDS Pharma Services, Phoenix International Life Sciences, and Bristol-Myers Squibb.
Dr. Farmen has in-depth knowledge of both large and small molecule bioanalysis, DMPK, regulatory strategies, and GLP/GMP regulations. He played a pivotal role at the Crystal City meetings which helped to shape the early regulatory landscape and guidelines for bioanalysis of pharmaceutical products.
Dr. Farmen earned his doctorate in pharmacology from Indiana University and did post-doctoral research in Biochemistry at the Upstate Medical Center in Syracuse, New York.
As Vice President of Scientific Affairs, Dr. Morimoto is directly responsible for developing and deploying scientific, regulatory and medical expertise and advice to various biotech and emerging pharmaceutical companies. He works closely with subject matter experts across all Celerion business units to provide consulting services and timely input on drug development programs.
Prior to joining Celerion, he was Vice President of Drug Development at Allon Therapeutics, where his responsibilities included management of early clinical research, nonclinical and manufacturing activities for the davunetide drug development program. Dr. Morimoto also directed the chronic/neuropathic pain program at NeuroMed Technologies. He started his career on the faculty in the Chemistry Department at Purdue University where his independent research focused on the regulation of signal transduction and second messenger production.
Bruce earned his doctorate in biochemistry from the University of California, Los Angeles (UCLA), and completed post doctorate research at University of California, Berkeley. He has a Bachelor of Science degree in biochemistry from the University of California, Los Angeles (UCLA).