Full-Time
Public academic health center educating, researching.
$44k - $47k/yr
Worcester, MA, USA
In Person
Bachelor's, Master's
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UMass Chan Medical School operates as a public academic health sciences center that trains healthcare professionals, conducts biomedical research, and provides consulting services to government and nonprofit agencies. Through its MassBiologics division, it functions as the only nonprofit, FDA-licensed manufacturer in the U.S. to develop and produce vaccines and monoclonal antibodies. This integration of a graduate school with a large-scale manufacturing facility allows the institution to move medical discoveries directly from the lab to public production. The organization's goal is to advance medicine and improve community health by combining education, clinical trials, and specialized care management.
Company Size
5,001-10,000
Company Stage
Grant
Total Funding
$182.6M
Headquarters
Worcester, Massachusetts
Founded
1962
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First mRNA flu shot approved by FDA bodes well for improving drugs of the future - though a few hurdles remain before... * Technology * 7 Aug 2026 4:24 am AEST * Share Vaccines have been reliably and affordably protecting people from diseases worldwide for centuries. Until the COVID-19 pandemic, however, vaccine development was still a long and idiosyncratic process. Traditionally, researchers had to tailor manufacturing processes and facilities for each vaccine candidate, and the scientific knowledge gained from one vaccine was often not directly transferable to another. * Li Li Assistant Professor of Biomedical Sciences, UMass Chan Medical School But the COVID-19 mRNA vaccines brought a new approach to vaccine development. And on Aug. 5, 2026, the U.S. Food and Drug Administration approved another mRNA vaccine - a seasonal flu vaccine for adults age 50 or older - that offers more protection against influenza compared to standard vaccines. These advances demonstrate the momentum of mRNA technology, and they have far-reaching implications for how researchers make drugs to treat many other diseases. Although there are many possibilities for what researchers can use mRNA to treat, some important limitations remain. My work as a biochemist and my lab at UMass Chan Medical School focus on developing better ways to use mRNA as a drug. Better understanding how mRNA-based drugs interact with the immune system and how they are degraded in human cells can help lead to safe, durable and effective treatments for a wide range of diseases. Some basics of mRNA drugs. Messenger RNA, or mRNA, is made of four building blocks denoted by the letters A, C, G and U. The sequence of letters in an mRNA molecule conveys genetic information that directs how a protein is made. Discover more Newspapers An mRNA drug comprises two essential components: mRNA molecules, which code for desired proteins, and the lipid molecules - such as phospholipids and cholesterol - that encapsulate them. These mRNA-lipid nanoparticles, or LNPs, are tiny spheres about 100 nanometers in diameter that protect mRNA from degradation and facilitate its delivery into target cells. Once inside cells, mRNA molecules instruct the cell's machinery to produce the target protein required for a desired therapeutic effect. For example, the mRNA in the Pfizer-BioNTech and Moderna COVID-19 vaccines directs cells to produce a harmless version of the virus' spike protein that trains the immune system to recognize and better prepare for potential infection. From a drug development perspective, mRNA drugs offer significant advantages over traditional drugs because they are easily programmable. Hundreds of pounds of mRNA can be made from readily available DNA templates, such that producing a different mRNA drug is as simple as changing the corresponding DNA templates. More importantly, different mRNA drugs produced by the same set of methods will have similar properties. They will be delivered to the same tissues, trigger similar levels of immune responses and degrade in similar ways. This predictability significantly reduces the development risks and financial costs of developing mRNA drugs. In addition to being easy to program, mRNA drugs have several other unique properties. For example, just like the mRNAs your body naturally produces, therapeutic mRNAs have a short half-life in cells: about one day. As a result, current mRNA technology is ideal for treatments that aren't meant to last long in the body. Discover more Government Beaches & Islands This is why vaccines are popular candidates for mRNA technology: They provide long-term protection against disease after brief exposure to the drug with few side effects. Self vs. nonself. Another critical feature of mRNA drugs is their intrinsic ability to stimulate the immune system. This may sound paradoxical - after all, your cells already contain large amounts of mRNAs. Why would other mRNAs activate your immune system? How does your immune system distinguish between self and nonself mRNAs? The first reason involves location. Therapeutic mRNAs enter cells using endosomes - sacs made of the cell's membrane that take in materials from the cell's environment. Your immune system can detect mRNA in endosomes because this is usually a sign of an RNA virus infection - cellular mRNAs normally don't enter endosomes. When your immune system labels therapeutic mRNAs as viral material, it triggers a strong inflammatory response that can lead to severe side effects. One solution to this problem is to modify mRNA's building blocks - specifically, changing the U, or uridine, to its chemical cousins, pseudouridine and N1-methylpseudouridine. This subtle chemical change prevents the unwanted immune response while allowing the therapeutic mRNA to direct the cell to make the protein it encodes. The 2023 Nobel Prize in physiology or medicine was awarded to the scientists who made this breakthrough discovery. Both the Pfizer-BioNTech and Moderna COVID-19 mRNA vaccines use this technique. The second source of unwanted immune response is impurities from mRNA production. To prepare mRNA from a DNA template, scientists use a protein called RNA polymerase that tends to make a small amount of side product called double-stranded RNA. Unlike mRNA, which is single-stranded, double-stranded RNA has two chains that form a double helix. RNA viruses also form double-stranded RNA when they replicate, and exposing cells to double-stranded RNA can lead to a strong immune response. Discover more Southeast Asians & Pacific Islanders Travel Guides & Travelogues Executive Branch Removing double-stranded RNA is challenging, especially at the industrial scale. Fortuitously, for mRNA vaccines, the residual amount of double-stranded RNA can stimulate the immune system to enhance antibody responses. However, for applications other than vaccines, a cleaner RNA product is necessary to reduce side effects. Moving beyond vaccines. Although mRNA has the potential to transform drug development for various medical purposes, careful consideration is required to identify targets that align with the technology's strengths. For example, because there is currently a limit to how long mRNA can last in the body, treatments that need a protein to be present for only a short period of time to achieve a lasting therapeutic effect are ideal. One promising example in development is using mRNA that encodes CRISPR-Cas9 gene-editing proteins to knock out genes that cause specific diseases. Researchers are exploring this strategy to develop a single-dose treatment for hereditary transthyretin amyloidosis, a rare genetic disease caused by the accumulation of misfolded proteins in the heart and nerves. This disease is an ideal target for mRNA-based CRISPR gene therapy because the target protein is produced by the liver. Because most drugs pass through the liver, this makes it easier to deliver CRISPR-Cas9 mRNA to its target. In the next few years, a new generation of more precise mRNA-based genome editing therapies will enter clinical trials. For treatments that need a specific protein to be present in the body for long periods of time or need to prompt little to no immune reaction, further advancements in mRNA technology are necessary to extend mRNA's half-life and eliminate immune-triggering contaminants. Notable new developments in these areas include using computational algorithms to optimize mRNA sequences in ways that enhance their stability and engineering RNA polymerases that introduce fewer side products that may cause an immune response. Further advancements have the potential to enable a new generation of safe, durable and effective mRNA therapeutics for applications beyond vaccines.
Terray appoints Lisa L. Decker, Ph.D. as Chief Business Officer. Ms. Decker brings deep expertise in building high-impact biotech partnerships to Terray Jun 15, 2026 Terray Therapeutics (www.terraytx.ai (http://www.terraytx.ai)) announced today the appointment of Lisa L. Decker, Ph.D., as Chief Business Officer. With 20+ years of biotechnology leadership and business development experience, Ms. Decker will lead the company's business development strategy as Terray capitalizes on the multiple opportunities enabled by its industry-leading drug discovery platform, EMMI. EMMI combines precise, proprietary data at scale with full-stack AI to rapidly identify and optimize structurally novel medicines. "Since our founding, we've known that AI could transform drug discovery, and now we're realizing that vision. EMMI is affording us a rich internal pipeline that should enable us to enter the clinic multiple times in the coming years and is delivering for our pharma partners on their programs," said Jacob Berlin, CEO. "Lisa will be an incredible asset and catalyst for our next stage as we evaluate opportunities for our medicines and continue to expand the impact of our platform across the pharma ecosystem. She brings together sophisticated business and science acumen alongside a mission-driven approach to building successful partnerships. I'm thrilled to have her on board." Ms. Decker added that "Terray's proprietary drug discovery platform has shown the ability to both deliver for partners on their challenging targets and build a proprietary pipeline of small molecule therapeutics for patients with autoimmune disease, which is incredibly exciting. I look forward to working with the Terray team and contributing to the mission of bringing new treatment options to patients." Most recently, Ms. Decker was Chief Business Officer at IGM Biosciences, where she oversaw business development, alliance and program management, and intellectual property functions. She served on the board of directors of Chimerix, Inc., until its acquisition by Jazz Pharmaceuticals in 2025. Prior to her role at IGM Biosciences, Ms. Decker was Chief Business Officer at Atreca, Inc., where she led business development and alliance management. She joined Atreca from Nektar Therapeutics, where she had served in multiple roles spanning business strategy and operations, program leadership, and business development and alliance management. Earlier in her career, Ms. Decker served as Associate Director in the Office of Technology Management at the University of Massachusetts Medical School. Ms. Decker received her Ph.D. in Immunology from Tufts University School of Medicine and her B.A. in Biology from the College of the Holy Cross. About Terray Terray is a chemistry-first, AI-native biotechnology company built at the intersection of AI and experimentation. Based in Los Angeles, the company is developing transformative small-molecule medicines for an internal immunology pipeline and across multiple other therapeutic areas with pharma partners. www.terraytx.ai (http://www.terraytx.ai)
David D. McManus appointed chancellor of UMass Chan Medical School. President Meehan calls Dr. McManus the perfect leader to guide his alma mater into the future. By UMass Chan Medical School Communications April 07, 2026 David D. McManus, MD'02, SMc'12, MBA, the Richard M. Haidack Professor in Medicine, chair and professor of medicine, renowned clinical and research cardiologist, and expert in digital medicine, was named incoming chancellor of UMass Chan Medical School today. The University of Massachusetts Board of Trustees unanimously approved UMass President Marty Meehan's nomination of Dr. McManus at a special meeting on Tuesday, April 7. He will be the first alumnus to lead UMass Chan. "Dr. McManus is the right leader to guide UMass Chan Medical School into the future," said Meehan. "His pioneering work in digital health care and AI, his deep experience in both the clinical and research fields, and his vision and collaborative nature, reflect the very best of UMass Chan." "It is always exciting when the best candidate is not only deeply familiar with the opportunities and challenges of the university, but is a product of it," said UMass Board of Trustees Chairman Stephen Karam. "Because of his background, experience and character, Dr. McManus is simply the best person to lead UMass Chan during this period of immense transformation in medicine, society, research and medical education." "As a graduate and a faculty member, I am deeply honored by the opportunity to serve as a steward of this world-class medical school," said McManus. "The groundbreaking discoveries that happen in laboratories at UMass Chan Medical School, in the classroom and at the bedside, are life-changing, and I will work tirelessly alongside the exceptional faculty, staff, students and community to continue advancing together. This institution has given me so much professionally and personally, and I will lean into this role with every fiber of my being to guide this institution through this moment of enormous change in medicine, education and society." McManus leads delivery of innovative and high-quality patient care, education programs, and transformative basic and clinical research. As chair of medicine, he oversees 16 divisions, more than 370 faculty members, 80 principal investigators and more than $70 million in annual research funding. He has built a culture of innovation and excellence that has made UMass Chan a destination for top academic talent, while expanding research programs and improving the department's overall performance. He is the founding director of UMass Chan's Program in Digital Medicine, has secured more than $140 million in NIH funding and published more than 400 scientific papers. He also leads efforts to train the next generation of health care innovators through programs funded by the NIH and the Commonwealth of Massachusetts. He was the principal investigator on the Rapid Acceleration of Diagnostics, known as RADx, grant, awarded by the NIH during the COVID-19 pandemic to bring innovative strategies for testing. He has earned recognition as a 2026 Innovator in Healthcare by the Boston Business Journal. McManus completed his internal medicine residency at the University of California San Francisco before returning to UMass Chan, where he completed a cardiovascular medicine fellowship and a clinical cardiac electrophysiology fellowship. He earned a master's degree in clinical investigation from UMass Chan in 2012 and an Executive MBA from MIT's Sloan School of Management in 2025. He is a native of Acton, Massachusetts, and earned his undergraduate degree from Brown University. "This search was comprehensive, inclusive and selective," said UMass Trustee and UMass Chan Chancellor Search Committee Chair David Brunelle. "The caliber of candidates drawn to this role speaks to the strength and national reputation of UMass Chan Medical School. Dr. McManus advanced through that process because the search committee saw in him what virtually everyone who works with him sees: a visionary leader who cares deeply about the Medical School and the people it serves. He is someone who will do everything in his power to lead it through its next evolution." "I applaud President Meehan and the Board of Trustees' appointment of David McManus to serve as the next chancellor of UMass Chan Medical School," said Michael F. Collins, MD, senior vice president for the health sciences and chancellor of UMass Chan. "It's an important moment in the history of an institution when a distinguished alumnus can assume this most important leadership position of his alma mater. I am heartened by Dr. McManus' selection, and I pledge my full support during and after our transition as his success and the success of UMass Chan remain my foremost and enduring priority." "The history of partnership and innovation between UMass Memorial Health and UMass Chan Medical School is unparalleled, guiding generations of clinicians through the journey of learning how to serve others with compassion, excellence, humility and an understanding of what's possible through innovation. We can't imagine a more talented and thoughtful leader to undertake the role of chancellor than Dr. David McManus, who has already left an indelible mark on the lives of countless patients throughout Central Massachusetts," said Eric Dickson, MD, president and CEO of UMass Memorial Health. "I look forward to working with Chancellor McManus to strengthen the ties that bind our institutions to achieve even greater feats for academic medicine and the future of clinical care." "After meeting a number of excellent candidates as part of the search process, I am confident Dr. McManus brings exceptional experience and a strong vision for leading UMass Chan in its next chapter. I'm looking forward to strengthening the partnership between UMass Chan and UMass Amherst on behalf of the common good," said Javier A. Reyes, chancellor of UMass Amherst and member of the search committee. McManus will succeed Collins, who announced in June 2025 that he would step down from his role as chancellor in June 2026 after serving for nearly 20 years. At the special Board of Trustees meeting, Meehan said of Collins: "By any measure, UMass Chan has thrived under the leadership of Chancellor Collins. He guided UMass Chan Medical School during a period in which it transformed into one of the very best medical schools in the country for primary care education, for research and for its service to its home state. He has left a lasting mark on this institution and on all the people who learn, teach, discover, research and innovate here." About the Search Process In October 2025, Karam and Meehan appointed a distinguished and broadly representative group of health care professionals, UMass faculty, business leaders, community stakeholders and alumni to lead a comprehensive search for the next chancellor of UMass Chan. Worcester area resident and UMass Trustee David Brunelle, co-founder and managing director of North Pointe Wealth Management, chaired the search committee. The search committee received input from a wide range of university stakeholders, including community leaders, students, faculty, staff and alumni throughout the search process. National executive search firm Isaacson Miller, which aided in the search process, reviewed more than 100 candidates, and the search committee interviewed the top 10. On Monday, March 30, the search committee unanimously voted to recommend four finalists to Meehan, indicating that all four were qualified and capable to lead the Medical School. One finalist subsequently withdrew from consideration. Meehan organized campus visits for three finalist candidates to solicit feedback from the UMass Chan community before making his recommendation to the Board of Trustees.
UMass Chan ranks 1st in Massachusetts for primary care education. By Tom Marino | April 7, 2026 Last Updated: April 7, 2026 WORCESTER - UMass Chan Medical School ranked first in Massachusetts for primary care education and second for research, according to U.S. News & World Report's 2026 Best Grad School Rankings. UMass Chan ranked ahead of the medical schools at Tufts, Boston University, and Harvard for primary care education and behind only Tufts for research. U.S. News ranked both UMass Chan and Tufts as tier two schools for both primary care education and research nationwide. Only 16 schools received tier one designation in both the primary care education and research categories. The Umass Chan Doctor of Nursing Practice program ranked 29th among 154 programs, while its PhD program ranked 55th among 159 doctoral programs in the biological sciences. This year, 61 students, or 35 percent of the T.H. Chan School of Medicine's graduating class, matched into residencies in primary care and related specialties. Those specialties include internal medicine, family medicine, and pediatrics. Graduates of the class of 2026 are the first class to complete all four years of the school's Vista curriculum, which UMass Chan introduced in 2022. The curriculum includes a health system science pillar, biomedical and clinical science pillars, and incorporates health equity, diversity and inclusion, population and community health, and patient and provider wellness into students' studies.
Phase I study for human monoclonal antibody for Lyme disease demonstrates safety, tolerability, pharmacokinetics. By Jim Fessenden March 31, 2026 A Phase I clinical trial of a human monoclonal antibody discovered and developed at UMass Chan Medical School for the prevention of Lyme disease in the U.S. was well tolerated and showed lasting serum concentrations in participants, according to data presented by Mark Klempner, MD, at the World Vaccine Congress 2026 in Washington D.C. TNX-4800 (formerly known as mAb 2217LS), a long-lasting borreliacidal (or bactericidal) was licensed to Tonix Pharmaceuticals Holding Corp., a commercial biotechnology company in Berkeley Heights, N.J. An adaptive Phase 2 field study is expected to begin in the first half of 2027, pending FDA clearance. "Our study demonstrated potentially protective blood levels of TNX-4800 at two days, with protective blood levels sustained for at least four months due to its extended half-life design," said Dr. Klempner, professor of medicine. "Additionally, with its differentiated mechanism of action, TNX-4800 has the potential to provide passive immunity by directly supplying neutralizing antibodies, bypassing the need for a vaccine to induce a patient's immune system to generate its own antibodies, which can be associated with other issues. We look forward to further clinical investigation of TNX-4800 as we strive to overcome this major public health challenge." Lyme disease, the most common tick-born illness in the Northern hemisphere, is transmitted to humans through the bite of infected deer ticks (Ixodes scapularis). According to the Centers for Disease Control and Prevention estimates, there are more than 450,000 cases annually in the U.S. That number is expected to rise as global changes in climate are expanding habitat range for ticks and other disease vectors. Typical symptoms of Lyme disease include fever, headache, fatigue and a characteristic skin rash called erythema migrans. If left untreated, infection can spread to the joints, heart and nervous system. While most cases of Lyme disease can be treated successfully with antibiotics, the only way to prevent infection is to avoid tick bites by using insect repellent and removing ticks promptly. "TNX-4800 is expected to provide a preventative option to the 87 million people in the United States who are at high risk of contracting the disease because they live, work or vacation in a tick-endemic area," said Seth Lederman, MD, chief executive officer of Tonix Pharmaceuticals. "As a monoclonal antibody, we believe TNX-4800 offers significant advantages over vaccines in development. Lyme disease vaccines that elicit antibodies to OspA [a protein found on the outer membrane of the bacterium that causes Lyme disease] currently in development take more than six months to offer protection and require complex immunization schedules. A previously approved anti-OspA vaccine was withdrawn due to poor uptake, potentially relating to its complex immunization schedule," said Dr. Lederman. Lyme is not caused by the tick directly. It is caused by the bacterium Borrelia burgdorferi present in the gut of infected ticks. When an infected tick bites someone and begins to feed on their blood, Lyme-causing bacteria can slowly travel from the tick's gut to its salivary glands and then transfer to the site of the bite. TNX-4800 blocks the maturation of Borrelia burgdorferi in the mid-gut of infected deer ticks. This inactivates the bacteria in the tick before it ever reaches the skin at the site of the tick bite. Intended to be administered in the early spring before ticks are at their most active, TNX-4800 is expected to provide almost-immediate protection from Borrelia burgdorferi bacteria-caused Lyme disease. A single injection is designed to maintain protective antibody serum concentration, with expected duration of protection approximately four months, providing pre-exposure protection against Lyme without relying on the recipient's immune system to generate antibodies. The primary objective of the Phase 1 study was to evaluate the safety and tolerability of a subcutaneous injection of TNX-4800 when administered to healthy male and female subjects 19 to 65 years old. The secondary objective was to evaluate pharmacokinetics when administered to healthy subjects. A total of 44 subjects were enrolled in the study, with 41 completing it. Results showed no significant clinical or laboratory safety signals with most adverse events mild or moderate. Pending FDA clearance, Tonix plans to initiate a randomized, double-blind, placebo-controlled, adaptive Phase 2 trial in the first half of 2027.