Meet the 2018 CARE Awards Judges
Judges for the 2018 CARE awards will be announced shortly.
The judging panel is comprised of independent, senior industry experts from around the world. They judge categories relevant to their areas of specialism and score against the published criteria. Each category is reviewed by at least three judges.
CARE awards 2017 judges:
Jeffrey M. Bockman, PhD
Vice President, Defined Health
Jeff leads the Oncology and Virology Practices at Defined Health. Jeff has extensive commercial and strategic perspective on the pharmaceutical and biotech industries. He has directed hundreds of in-depth licensing opportunity and valuation assessments during his tenure at DH. He often speaks at conferences on scientific and commercial issues in cancer, especially immuno-oncology.
Before joining Defined Health, Jeff was a Senior Research Scientist and Research Project Leader in the commercial development of oligonucleotide therapeutics for viral diseases and cancer at Innovir Laboratories; and an Assistant Research Professor at The George Washington University School of Medicine. He has worked closely with two Nobel Prize recipients: Dr. Sidney Altman on ribozymes, and Dr. Stanley Prusiner on prions, and holds four patents in the use of ribozymes.
He received a BA from University of California at San Diego, a PhD in Medical Microbiology from the University of California at Berkeley, and an MA in English/Creative Writing from New York University.
Jeff is a member of the Licensing Executives Society (LES), the American Association for Cancer Research (AACR), the American Society of Clinical Oncology (ASCO), the American Society of Hematology (ASH), and the American Society of Gene and Cell Therapy (ASGCT).
Pharmaceutical Training Consultant, Course Director, University of Cardiff
Dr Laura Brown is Course Director of the MSc in Clinical Research, University of Cardiff and a Training and QA Consultant.
Dr Brown has held a number of international and senior management positions in the pharmaceutical industry. She has worked for several international companies including GlaxoWellcome, Hoechst Marion Roussel and Phoenix International.
She was a member of the Editorial board of the Good Clinical Practice Journal for 10 years. She is author of several books including Project Management for the Pharmaceutical Industry, a Practical Guide to the Clinical Trial Directive and several articles on the new EU Clinical Trial Regulation.
Denis Curtin PhD
Chief Scientific Officer, mProve Health
Denis Curtin, Ph.D., co-founder and Chief Scientific Officer for mProve Health, a technology company specializing in digital solutions for clinical research and commercial healthcare. mProve Health is the global leader in innovative mobile solutions for clinical trials and consumer disease management. Experience includes: twenty years of pharmaceutical industry roles in drug and vaccine development and commercial brand management, brand creation and development, market analysis, product lifecycle and franchise strategic planning, and clinical trial design and management.
Director of Sponsored Research Programs & Research Associate Professor, Tufts Center for the Study of Drug Development
Kenneth A. Getz is the chairman of CISCRP – a nonprofit organization that he founded to educate and raise public and patient awareness of the clinical research enterprise. He is also the Director of Sponsored Research and an associate professor at the Tufts Center for the Study of Drug Development, Tufts University School of Medicine where he conducts research programs on drug development management strategies and tactics, outsourcing, global investigative site and patient recruitment practices and policies. Ken has twice been nominated for a Distinguished Faculty award at Tufts University. A well-known speaker at conferences, symposia, universities, investor meetings and corporations, Ken has published extensively in peer-review journals, books and in the trade press. He holds a number of board appointments in the private and public sectors. He is currently a board member of WCG and the Metrics Champion Consortium, LLC; on the editorial boards of Pharmaceutical Medicine and Therapeutic Innovation and Regulatory Science; and writes a bi-monthly column nominated for a Neal Award in Applied Clinical Trials. Ken holds an MBA from the J.L. Kellogg Graduate School of Management at Northwestern University and a bachelor’s degree, Phi Beta Kappa, from Brandeis University. Ken is the founder of CenterWatch, a leading publisher in the clinical trials industry.
Laurie A. Halloran, BSN, MS
President, Halloran Consulting
Ms. Halloran is the President of Halloran Consulting Group (HCG), founded in 1998 with the vision of Life Science Product Development that Works; Product, Process and People. With over 30 years in senior clinical affairs management and process optimization, including both biopharma (Oxigene and Antigenics), and CROs (PAREXEL), Ms Halloran has become recognized as an industry expert.
In 2015, Laurie was honored by the Boston Business Journal as a Woman of Influence, and the company has received a ranking in the INC 500 fastest growing companies for the past 2 years. In 2010, Laurie was selected as one of the 100 Most Inspiring People in Life Science by PharmaVoice and in 2009, she was awarded Clinical Researcher of the Year by ACRP’s New England Chapter.
President, C. Kalb & Associates
Cliff Kalb is President of C. Kalb & Associates, LLC, a pharma consultancy in intelligence and strategy. He has served for over four decades in a broad variety of senior level functions the industry. Cliff was Senior Vice President with Wood Mackenzie, where he provided thought leadership on life science industry issues and directed their knowledge based research and consulting practice. Previously, he served as Senior Director, Strategic Business Analysis at Merck, heading their global intelligence function. Earlier in his career he worked for Marion, Pfizer, and Roche in sales, market analysis, health economics, public policy, marketing, licensing, business intelligence and business development building experience across virtually all therapeutic categories. He also headed commercial development for a biotechnology firm affiliated with J&J.
Director, Center for Integration of Science and Industry, Bentley University
Fred D. Ledley, M.D. is Professor of Natural & Applied Sciences and Management, and Director of the Center for Integration of Science and Industry, at Bentley University. A recognized innovator, entrepreneur, and executive, he has led successful research programs, start-up companies, and progressive academic change. His current research focuses on characterizing business models for translational science and developing strategies for more efficient translation of scientific discoveries to create public value. Dr. Ledley has served on the faculties of the Baylor College of Medicine and the Howard Hughes Medical Institute, and was involved in founding several biotechnology companies including GeneMedicine (NASDAQ:GMED), and Variagenics (NASDAQ: VGNX). He has served on the Board of Directors of the Massachusetts Biotechnology Council, the Board of Overseers of Boston Children’s Hospital, and as a consultant to industry, academia, and government. He has published widely in fields ranging from gene therapy and genomics, to bioethics, science, education, biotechnology, and business strategy. His first novel, Sputnik’s Child, recalls the events that shaped the ideas and lives of the baby boomer generation and laid the groundwork for an age of technology and its challenges.
Senior VP of BD and Alliance Management, Heat Biologics
Janice Marie McCourt, RPh, MBA has 20+ years of experience leading pharma and biotech companies in the United States and internationally, working across the R&D-to-commercial continuum. Janice has the unique ability to combine cutting-edge science with business acumen having raised over $3 billion in global value-creating licensing, acquisition, and partnership deals with top tier pharmaceutical and biotechnology partners. Janice led the strategic and tactical diversification of Agenus from a vaccines-focused company directly into the antibody check point modulation space with the acquisition of 4-Antibody, thereby establishing the company as a leader in immuno-oncology.
She enabled Praecis, Amakem Therapeutics, and ActivBiotics to raise over $415M in Series A, B, IPO and secondary financings to position those companies for clinical and commercial success. (Praecis was a top 10 IPO on Wall Street). She has led over 100 product launches for major brands in immuno-oncology, CNS, immunology, inflammation, women’s health, neurology, respiratory, ophthalmology, infectious disease, vaccines, pain and numerous therapeutic areas. She has repeatedly demonstrated how to combine innovative scientific vision with sound business strategy.
Alison Messom PhD MICR
Chairman of the Board of Directors, Institute of Clinical Research
Since 2012 Dr Alison Messom has been Chairman of the Institute of Clinical Research; the oldest independent membership lead professional body for global clinical researchers. With a background in molecular Genetics, Dr Messom has almost 20 years industry experience working both within Pharmaceutical Companies and Clinical Research Organisations. Dr Messom has detailed experience of directing global clinical trials and has worked in a wide variety of leadership roles, within Pharma Companies & CROs for not only project and monitoring teams, but also Data Management, Outsourcing, Informatics and Translational Medicine Departments. Most recently she has provided consultancy support to an academic group working on a translational medicine project and operational consultancy to a mid-sized pharma company working in phase III & IV.
Managing Director, The Trout Group
Chad Rubin is a Managing Director for the Trout Group and Trout Capital. Trout is the leading investor relations and capital markets advisory firm dedicated to the life science industry. Chad has over 16 years of experience advising management teams in the sector. Prior to joining Trout’s team in 2005 Chad was the head of Biotechnology Capital Markets Intelligence Group at Thomson Financial, assisting over 100 life sciences companies in their understanding of Wall Street. He brings with him experience in advising life science companies on topics including company creation, seed funding, shareholder targeting, capital markets transactions, message crafting and scenario analysis. His experience includes work in finance, consulting and market analysis. He has been involved with companies from the pre-IPO stages to follow-on and convertible offerings. He is involved in capital transactions with corporate clients and has counseled clients on domestic and cross-border transactions and binary data events.
Chad holds a Bachelor of Arts degree in business administration with a concentration in finance from Franklin & Marshall College. He has a minor in film and media studies. He also holds Series 7, 79 and 63 securities licenses.
Chad, who now sits on the Board of Trustees for the Histiocytosis Association, began volunteering with the HA in 2008 after his son, Jack, was diagnosed with Langerhans cell histiocytosis and secondary HLH. Jack and Chad’s wife, Kristy, lived at Children’s Hospital of Philadelphia for over 19 months fighting the diseases. Jack was cured with a bone marrow transplant and is a healthy boy today! Histiocytosis Association provided Chad with support, information and resources to help his family fight and beat the horrible disease. Chad and Kristy founded the annual fundraiser “All Jacked Up” in 2009. Together with friends and family they have raised over $800,000 to help find a cure.