About Rallybio

Rachael Alford, PhD

Rachael has more than 15 years of biopharmaceutical industry experience in all aspects of technical operations. Most recently, she served as Vice President of Global Process Development at Alexion Pharmaceuticals, where she led biologic and small molecule development, early and late stage process development, analytical and formulation development, tech transfer, regulatory submissions and life cycle management. 

Rachael earned both her B.Sc. in Chemistry and PhD in Biophysical Chemistry from Imperial College, London, and was a Postdoctoral Research Associate at Yale University.

Róisín Armstrong, PhD

Róisín has over 25 years of biopharmaceutical industry experience, specifically in advancing products through the development continuum to commercialization. Most recently, she served as Vice President and Global Medicine Team leader at Alexion Pharmaceuticals, where she led teams in the development and registration of new treatments for rare and ultra-rare neurology indications. In 2019, Róisín was the recipient of an HBA Luminary Award by the Healthcare Businesswomen’s Association. Prior to Alexion, Róisín worked with Pfizer in the UK and the US in various roles of increasing responsibility, including early and late-stage Development Portfolio Operations and global clinical leadership roles in different therapeutic areas. 

Róisín received her PhD in Neuropharmacology from the University of Wales, College of Cardiff, having previously obtained a BSc in Pharmacy from DeMonfort University in Leicester, UK.

Zubin Bhagwagar, MD, PhD

Zubin is a physician scientist with more than 25 years of experience in academia and the pharmaceutical industry. Prior to joining Rallybio, Zubin was Vice President External Innovation at Alexion Pharmaceuticals, and led the Strategic Evaluation team in Business Development. He previously held positions of increasing responsibility at Bristol-Myers Squibb, where he worked in multiple therapeutic areas including neuroscience and clinical pharmacology. Zubin received his medical degree and completed his first psychiatry residency at Delhi University; he subsequently completed clinical training in psychiatry and neuroscience at the University of Oxford, where he was awarded a D.Phil (PhD) in neuroimaging and neurobiology. He is a Fellow of the Royal College of Psychiatrists, U.K., has authored more than 80 papers in neuroscience/psychiatry and has been on the faculty at the Department of Psychiatry at Yale University School of Medicine since 2005, where he is an Adjunct Associate Professor.

Michael Bombara

Michael brings over 30 years of clinical operations experience to Rallybio. He spent over 20 years at Alexion Pharmaceuticals in clinical operations, most recently serving as Executive Director of Clinical Business Operations, where he oversaw the strategic planning of clinical, scientific, and operational aspects of numerous clinical trials. Prior to Alexion, Mike spent 10 years in pharmaceutical sciences at Bayer and 4 years at Genentech, conducting bench research in immunology, metabolic, and rheumatic disorders.

Mike received a Bachelor of Science in Microbiology from the University of Maine.

Dominic Carrano CPA, MSA

Dominic is a Certified Public Accountant with more than 10 years of experience managing areas of technical accounting and financial reporting. Prior to joining Rallybio, he served in roles of increasing responsibility at Alexion Pharmaceuticals, most recently as Associate Director of Technical Accounting.  In this role he oversaw the implementation of new accounting standards, technical accounting assessments, forecasting and modeling, external reporting disclosures, and lent his expertise in these areas to various strategic projects. Dominic began his accounting career at Deloitte & Touche.

Dominic earned his Master of Science and Bachelor of Science in accounting from the University of Connecticut.

Laura Ekas, PhD

Laura has more than 10 years of experience in the biotech industry. Her broad background includes experience in global pricing and reimbursement, corporate operations and investor relations at Alexion Pharmaceuticals. Prior to her time at Alexion, Laura spent time in healthcare strategy consulting and also held positions of increasing responsibility at Canaccord Genuity Group, including Vice President, Biotech Equity Research. She has a PhD in pharmacology and signal transduction from New York University, School of Medicine and a B.A. in behavioral biology from Johns Hopkins University.

Jeffrey Fryer, CPA

Jeff is a co-founder of Rallybio and has more than 25 years of experience in business finance and the economics of operations, as well as corporate strategy and taxation.  He has held leadership roles at Alexion Pharmaceuticals, Chemtura Corporation, and Lydall, and began his career in public accounting with PricewaterhouseCoopers.  He earned a Master of Science in taxation from the University of Hartford and a Bachelor of Science in business administration with a concentration in accounting from Bryant University.  He is a member of the Dean’s Advisory Council for the Bryant University School of Business.

Michael Greco, JD

Mike has more than 20 years of legal and business experience, including in private practice and as a member of life science leadership and executive management teams. Prior to joining Rallybio, Mike served as General Counsel and Secretary for SpringWorks Therapeutics where he helped facilitate the successful implementation of the company’s IPO, among other milestones and accomplishments. Previously, he held leadership roles at Alexion Pharmaceuticals where he assumed positions of increasing responsibility in the company’s legal department, oversaw corporate governance initiatives, public reporting and securities compliance and corporate transactions. He was also responsible for managing the legal department’s corporate, R&D, business development and employment law legal teams. Prior to Alexion, Mike was a corporate attorney at Wiggin and Dana LLP and Bingham McCutchen LLP (now Morgan Lewis).

Mike served in the U.S. Army Corps of Engineers and received a JD from Suffolk University Law School and a B.S. from the United States Military Academy, West Point.

Amanda Hayward, PhD

Amanda has 20 years of biopharmaceutical industry experience, specifically in venture capital, portfolio management, business development, and licensing transactions. Most recently, she served as Managing Director of Venture Investments for Connecticut Innovations, and is Chairman of Hoba Therapeutics. She has also played a significant role in founding and growing multiple companies.

Amanda earned her PhD in Cell Biology and Anatomy from Texas Tech University Health Sciences Center, and was a Postdoctoral Fellow at Yale.

Ann Houston, MA, PMP

Ann has more than 24 years of experience in drug discovery, development and project management expertise, including leadership positions at Inozyme Pharma and Alexion Pharmaceuticals. Ann has also held senior positions with increasing responsibility in project, portfolio management and therapeutic area strategy at Bristol Myers-Squibb and Pfizer, driving the delivery of medicines in all phases of development across a range of therapeutic areas.  Ann is a Certified Project Management Professional.  She received her M.A. in molecular biology and biochemistry from Wesleyan University. She also holds a B.S. in biology and a B.A. in chemistry from Providence College.

Lauren Kriss

Lauren has more than a decade of experience in managing accounting processes and financial reporting. Before joining Rallybio, she served as Assistant Controller responsible for managing annual external financial audit procedures and quarterly reviews for Trevi Therapeutics. She previously served as Manager, Financial Planning and Analysis at Spinewave, Inc., and as an Accounting Manager at Kolltan Pharmaceuticals, Inc. where she helped build and maintain annual and long-range budgets, forecasts and business planning models.

Lauren earned a B.S. in accounting from Central Connecticut State University.  

Zhiyao Lu, PhD

Yao was trained as a scientist with expertise in chemistry and pharmaceutical sciences. Before joining Rallybio, Yao was a Fellow at the Blavatnik Fund for Innovation at Yale, where he assessed early-stage life-science opportunities and helped with company formation. Prior to that, he served as the co-founder and CTO of Catapower Inc., a seed-stage company developing and commercializing technologies for anti-microbial materials. Yao began his career at Amphastar Pharmaceuticals, where he identified and evaluated new business development opportunities.

He received his B.S. in pharmacy and M.S. in medicinal chemistry from Peking University and earned a Ph.D. in chemistry from the University of Southern California.

Adam Lucka, MSc

Adam has more than 20 years of direct pharmaceutical development experience delivering innovative solutions and extensive program management involvement. Before joining Rallybio, he held several positions of increasing responsibility, more recently serving as Senior Director, Product Development Operations at Alexion Pharmaceuticals where he led the development of the CMC program strategy for multiple products in alignment with the overall program strategy, and managed budget forecasting and adherence.

Adam earned his MS in analytical medicinal chemistry from Purdue University and a BS in biology with a minor in chemistry from the University of Dayton.

Martin Mackay, PhD

Martin is a co-founder of Rallybio, and has worked in pharmaceutical and biotech R&D for more than 30 years, holding leadership roles at companies including Pfizer (NYSE: PFE), AstraZeneca (NYSE: AZN) and Alexion.  Martin obtained a First Class Honours Degree in microbiology from Heriot-Watt University and his PhD in molecular genetics from the University of Edinburgh. He is currently a member of the Board of Directors of Charles River Laboratories (NYSE: CRL) and Novo Nordisk (NYSE: NOVO), and is a Senior Advisor at New Leaf Ventures.  Martin summarizes the three loves in his life as being family, work, and soccer, but not necessarily in that order.

Michael Murphy, RPh

Michael has extensive experience in project, program and portfolio management with comprehensive expertise all phases of research and development, and business management practices. Before joining Rallybio, he made a career at Pfizer Inc., holding positions of increasing responsibility, most recently leading the governance management group, where he was chair of the body accountable for operational review of clinical programs, and led the team which delivered novel, optimized adjudication processes and decision engagement points.

Mike is a pharmacist and holds a Masters in Pharmacy Administration from the University of Rhode Island.

Kiran Patki, MD, MSc

Kiran brings over 20 years of clinical research and development experience to Rallybio, including the design and execution of global clinical trials in severe and life-threatening rare diseases indications. Prior to joining Rallybio, Kiran served as Vice President of Clinical Development at Gemini Therapeutics, where he led the Company’s clinical development programs. Before this, he held clinical development leadership roles at Aeglea BioTherapeutics as Vice President of Rare Genetic Disease Clinical Development and at Alexion as Senior Medical Director and Global Research & Development Team Leader. Kiran earned a Bachelor of Medicine & Bachelor of Surgery (M.B.B.S.) and MD from the University of Bombay, an MSc in Pharmaceutical Medicine from Hibernia College, and is board certified by the American Board of Clinical Pharmacology.

Steve Ryder, MD

Steve has more than 30 years of leadership experience in global healthcare development and a proven track record in the rare disorders space. Prior to joining Rallybio, Steve served as Senior Vice President, Chief Development Officer at Alexion Pharmaceuticals, where he led the global development, registration, and approval of new drug candidates for rare diseases, and contributed to the overall growth of the company. Previously, he was founding President, Astellas Pharma Global Development, and spent 21 years in development at Pfizer. Steve received his MD from the Icahn School of Medicine at Mount Sinai.

Jackie Schumacher

Jackie has more than 30 years of diverse experience in global regulatory affairs, development, commercialization and portfolio management from initial clinical investigation through registration. Prior to joining Rallybio, Jackie served as Vice President of Regulatory and Quality at Lyndra Therapeutics where she was responsible for regulatory strategy and operations and for overseeing the Company’s global GxP quality strategy and Quality Management System. Previously, she spent more than two decades in pharmaceutical sciences within Pfizer, starting as an analytical chemist followed by a long tenure within the Chemistry, Manufacturing, and Controls (CMC) regulatory organization. During her time at Pfizer, she developed and led successful global CMC registration strategies for new small molecules, product enhancements, and combination products, held regulatory leadership positions within the nascent Established Products Sterile Injectables organization and was responsible for helping to optimize the value of the company’s 600+ established molecule portfolio. She is currently on the board of directors for Women in the Enterprise of Science and Technology (WEST), a non-profit dedicated to the advancement of women in science, technology, and engineering. Jackie received a Bachelor of Arts in chemistry and classical studies from Hamilton College.

Douglas Sheridan, PhD

Doug has more than 20 years of R&D experience, both academically and professionally. He is a co-inventor of five clinical drug candidates, including an orphan drug approved by the FDA in 2018. Prior to joining Rallybio, Doug served as Executive Director, Global Program Team Leader at Alexion Pharmaceuticals, where he led the cross-functional development teams responsible for the strategy, budget and operational activities required to launch two global development programs. Doug earned his PhD in Neuroscience from Yale University. He also holds a B.S. in Biochemistry and Molecular Biology from Pennsylvania State University.

Lisa Sinclair

Lisa has more than 25 years of biopharmaceutical experience specializing in building and implementing portfolio strategy and new product development from pre-clinical to launch.  Prior to joining Rallybio, Lisa served as the Head of Program and Alliance Management for SpringWorks Therapeutics where she led operational planning, lifecycle strategies and alliance collaborations.  She previously served as Vice President of R&D Strategy, Portfolio and Project Management at Alexion and as the Vice President of Global R&D Portfolio and Performance at AstraZeneca.  Before this, Lisa spent 18 years at Pfizer in various roles of increasing responsibility in R&D, Portfolio Management and Commercial.  Lisa received a Bachelor of Arts in Business Administration with a concentration in Marketing from the University of Vermont.

Michael Sullivan, MBA, PMP

Michael has more than 20 years of biopharmaceutical experience, with expertise in project and portfolio management. Mike has been focused on driving R&D programs through all stages of development as well as improving operational performance of various R&D functions. Prior to joining Rallybio and most recently, he served as Senior Director of Drug Safety Operational Performance and Excellence at Alexion Pharmaceuticals where he led critical and transformative programs across the company’s pharmacovigilance organization. He also held positions of increasing responsibilities in R&D strategy, portfolio and project management at Alexion and Pfizer.

Michael is a Certified Project Management Professional. He earned his MBA from Lake Forest Graduate School of Management and holds a B.S. in industrial engineering from Iowa State University.

Samantha Tracy

Samantha has more than 10 years of experience in both public and corporate accounting. Before joining Rallybio, she served as Controller for RJ Health Systems, where she oversaw accounting operations, developed annual budgets and prepared financial forecasts, ensuring the fiscal welfare of the organization. Previously, she served as Director of Accounting at IsoPlexis Corporation and as a Senior Financial Analyst at HB communications.

Samantha earned a B.S. in Accounting from Stockton University.  

Steven Tuch

Steven brings over 30 years of financial experience to Rallybio, of which 25 years have been spent working with Life Science companies. Most recently, he served as Managing Director, Head of U.S. Equity Capital Markets Originations for BMO Capital Markets, where he was responsible for building the firm’s equity capital markets business. Prior to assuming that role, Steven spent seven years as the Head of BMO’s Health Care Equity Capital Markets practice. While at BMO, Steven completed over 140 transactions raising over $20 billion. Previously, he was a Managing Director at Deutsche Bank Securities in New York, where his roles included Head of Health Care Equity Capital Markets, Head of Consumer and Business Services Equity Capital Markets and Head of Equity Private Placements. Before Deutsche Bank, Steven ran the Equity Private Placement Group at Thomas Weisel Partners and was a Vice President at Montgomery Securities.

Steven received an MBA from Stanford University’s Graduate School of Business and a BBA from the University of Michigan.

Steve Uden, MD

Steve is a co-founder of Rallybio. He has more than 25 years of experience, serving in R&D leadership roles with prominent global pharmaceutical and biotech firms.  Steve was previously head of research at Alexion Pharmaceuticals where he led a series of collaborations and external alliances, expanded its research base beyond antibodies to include small molecules, RNA-based therapies and broader protein engineering capabilities.  Prior to Alexion, Steve led research and development groups in Japan for Wyeth and Novartis Oncology, and held positions of increasing responsibility at Pfizer in the U.K., Japan, and the U.S. Steve received his medical training at the University of London’s St. Thomas’ Hospital Medical School, and then practiced clinical and academic medicine within the U.K. National Health Service and the University of Manchester U.K.

Haren Vasavada, PhD

Dr. Vasavada has more than 25 years of experience as a scientist, manager, and R&D leadership team member in the areas of biopharmaceuticals, small molecule therapeutics, and research technologies. Prior to joining Rallybio, he served as the Head of New Targets and Therapeutics at Alexion Pharmaceuticals, and Vice President, Process Science at Optherion, Inc. He began his career in the biopharmaceutical industry at Bayer, Inc., where he rose to the position of Director of Research, Department of Research Technologies, advancing a both small molecule and biologic drug candidates into product development. Before his industry career, Dr. Vasavada was an associate research scientist in Yale University’s Department of Human Genetics. He received his PhD from the Indian Institute of Science in Bangalore and did his postdoctoral work at Yale University.

Eric Watsky, MD

Having held executive positions in pharmaceutical research and development, Eric also has extensive experience in patient care and academic research.  Prior to joining Rallybio, Eric served as Vice President, Global Development Team Leader for Alexion Pharmaceuticals, and Executive Director in Pfizer’s Specialty Care Business Unit focused on rare disease indications.  He was also Senior Staff Research Fellow at the National Institute of Mental Health.  Eric received his MD from Boston University and has taught at the medical schools of Harvard, where he was Chief Resident in Psychopharmacology, and George Washington University.

Carrie White

Carrie has a proven track record of leading and managing venture capital investments and strategic initiatives in the bioscience industry. She has held various positions with increasing responsibility for Connecticut Innovations, most recently leading or supporting 27 early-stage bioscience venture capital investment deals totaling more than $21M. Previously, Carrie worked for Pfizer specializing in clinical data management, before transitioning into a business operations role where she managed the budget development and reporting process for the statistical programming and medical writing departments. Carrie has also achieved her Six Sigma Green Belt. She received her MBA from Northeastern University and holds a B.S. in Public Administration from the University of Arizona.

Ting Yi, PhD, MBA

A scientist with expertise in biochemistry and molecular biology, Ting has valuable experience in business development. Before joining Rallybio, Ting was Director of Business Development for Tangen Biosciences Inc., where she managed a government project, led contract and license negotiations and cross-functional marketing efforts. Prior to that, she served as an Investment Associate at Connecticut Innovations bioscience venture, focused on sourcing new deal opportunities, managing portfolio companies and fund raising. Ting began her career as a Postdoctoral Associate at Yale University Medical School using stem cell techniques to investigate cardiac disease.

She received her B.S. in biological engineering and M.S. in biochemistry and molecular biology from Beijing Institute of Technology and earned a Ph.D. in molecular physiology and biophysics from the University of Vermont.