Patent Agent
Carolyn M. Boudreau, Ph.D., applies her robust scientific foundation in immunology, virology, and infectious diseases to intellectual property (IP) matters, with particular emphasis on biologics and vaccine technologies. Her experience spans academic research, industry innovation, and startup leadership, positioning her to support patent prosecution and IP strategy with deep technical insight and cross-functional collaboration.
Carolyn has extensive scientific expertise across academic and industry environments. She contributed to patent development and prosecution as a research scientist, including serving as a liaison between research teams and legal counsel to assess prior art, design patent portfolios, and evaluate freedom-to-operate (FTO) matters. Carolyn’s scientific work has supported the advancement of nasal spray therapeutics, antibody engineering, vaccine design, and nanobody discovery, with specific applications in pandemic preparedness and mucosal immunity.
Prior to entering the legal field, Carolyn led scientific programs in multiple startup environments. She independently developed a novel in vivo nanobody discovery platform, integrating cutting-edge wet lab techniques with artificial intelligence (AI)-driven bioinformatics. Working with an international team of scientists, business development professionals, and legal experts at a biotechnology company based in the Netherlands, she developed a drug discovery pipeline for nasal spray therapeutics to prevent infection with respiratory viruses. Her leadership in these environments extended to personnel management, operational oversight, regulatory compliance, and client engagement, including proposal development and project execution.
Carolyn’s doctoral research focused on functional humoral immune responses to influenza vaccinations, utilizing systems immunology approaches, in vitro and in vivo models, and machine learning (ML). She collaborated with industry partners on vaccine development and supervised junior researchers. Her work has been recognized with multiple publications in high-impact journals, including Nature Communications, Cell Reports Medicine, and Scientific Reports, and she has presented her findings at international conferences and symposia.
Coauthor, “Intranasal administration of a panreactive influenza antibody reveals Fc-independent mode of protection,” Scientific Reports, 2025.
Lead Author, “Antibody-mediated NK cell activation as a correlate of immunity against influenza infection,” Nature Communications, 2023.
Lead Author, “Pre-existing Fc profiles shape the evolution of neutralizing antibody breadth following influenza vaccination,” Cell Reports Medicine, 2023.
Lead Author, “Dissecting Fc signatures of protection in neonates following maternal influenza vaccination in a placebo-controlled trial,” Cell Reports, 2022.
Speaker, Maternal Antibody Transfer, Harvard T.H. Chan School of Public Health, 2020.
Lead Author, “Selective induction of antibody effector functional responses using MF59-adjuvanted vaccination,” The Journal of Clinical Investigation, 2020.
Award, Select Paper of the Year, Massachusetts General Hospital Graduate Student Division, 2019.
Presenter, Vaccine Discovery and Development, Keystone Symposia, 2018.
Winner, Healthy Lives Category, Merck Innovation Cup, 2018.
Finnegan is lead and preferred IP transactions counsel for one of the largest pharmaceutical companies in the world, handling more than 50 diligence projects each year, including all IP and related transactional aspects of the matters. The transactions span the full gamut of technologies from small molecule through biologics such as antibodies, oligonucleotides, and gene therapies. Finnegan also provides extensive assistance with post-deal integration procedures and subsequent global prosecution and portfolio strategy, ensuring a seamless transition of IP assets to the company and maximum value from acquired IP.
Global prosecution and portfolio management for major pharmaceutical company
Finnegan is lead and preferred IP strategy counsel for one of the largest pharmaceutical companies in the world, handling all aspects of prosecution and portfolio management for multiple top-tier products for the client. The work spans the gamut from drafting and prosecution through larger strategic planning, patent term extension, and pre-litigation preparation on blockbuster small molecule and biologic products in the oncology, rheumatology, immunology, neuromuscular, and cell and gene therapy spaces.
magna cum laude, 2014
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