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bruce carter 200BRUCE CARTER, PHD

Bruce Carter joined the IDRI Board of Directors in October 2014 and currently serves as chair. He began his career in drug discovery at G.D. Searle and later joined ZymoGenetics, Inc., where he served as president from 1988 to 1994 when Novo Nordisk acquired the company. At Novo Nordisk, Carter was Corporate Executive Vice President and Chief Scientific Officer until 2000 when he led a buyout of ZymoGenetics, establishing it as an independent company from Novo Nordisk.

He was named President and Chief Executive Officer and led ZymoGenetics' successful development and commercialization of Recothrom ®, a recombinant thrombin for use during surgical procedures. Bristol-Myers Squibb acquired ZymoGenetics in 2008. Most recently, Dr. Carter was Executive Chairman of Immune Design Corp. from 2009 to 2011.

In addition to being a member of IDRI's Board of Directors, Carter serves on a number of corporate boards, including Dr. Reddy's Laboratories Ltd., in Hyderabad, India.

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Bio-Steve-Cordial200C. STEPHEN CORDIAL, MBA

Steve Cordial joined the IDRI Board of Directors in January 2016 and serves as chair of the Finance Committee. For the past 11 years, he has served as president of Steve Cordial Consulting, where he has provided interim CFO support for a variety of companies, ranging from a private-equity owned personal care company with more than $400 million in revenues to a $29 million per year venture-backed telecom equipment manufacturer.

Prior to starting his own consulting firm, Cordial served as CFO and interim CEO at Somera Communications, CFO at Nexsi Systems, CFO at Xylan Corp. and CFO at Sierra Semiconductor. He started his career as a Division Controller at Texas Instruments.

He holds a BA in economics from Stanford University and an MBA from Santa Clara University. Cordial also works as a community volunteer and has developed experience in nonprofit accounting. He serves as a partner at Social Venture Partners Seattle and holds board positions at TeamChild and at the Kindering Center, where he serves as treasurer and as a member of the advocacy and governance committees.

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©Earl HarperSTEVEN G. REED, PHD

Founder, President & Chief Scientific Officer

Steve Reed is IDRI's Founder, President and Chief Scientific Officer. His academic appointments include Professor of Medicine at Cornell University Medical College in New York and Research Professor of Pathobiology at the University of Washington. He serves on several editorial review committees, has served as a member of the Tropical Medicine Review Board of the National Institutes of Health, and has served as a member of diagnostic and vaccine steering committees of the World Health Organization.

Steve received his PhD in Microbiology and Immunology from the University of Montana in 1979. That year he was appointed as Scientist of the National Institute of Amazon Research in Manaus, Brazil, where he directed research on tropical diseases. Steve joined Cornell University Medical College in 1980 as Assistant Professor of Medicine, continuing to work in Brazil as manager of the Cornell-Bahia program in International Medicine. He joined Seattle Biomedical Research Institute in 1984 where he worked until founding IDRI in 1993.

In 1994, he co-founded Corixa Corporation (which was later sold to GlaxoSmithKline, GSK) where he served as Chief Scientific Officer until leaving in 2004. In 2008 Steve co-founded Immune Design Corp. where he served as CEO until 2011.

Steve's research interests have focused on the immunology of intracellular infections, and on the development of vaccines and diagnostics for both cancer and infectious diseases. He led the team that, together with GSK, developed the first defined tuberculosis vaccine to advance to clinical trials, and has developed the first defined vaccines for leishmaniasis, as well as the K39-based diagnostic tests currently licensed for leishmaniasis.

Steve has more than 250 original publications, 40 book chapters and reviews, and 105 issued patents on diagnostics, vaccines, and therapeutics of infectious diseases and cancer.

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MassimoRadaelliMASSIMO RADAELLI, PHD

Massimo Radaelli has served on IDRI’s Board of Directors since June of 2012. He is the President and Founder of Noventia Pharma Specialty Pharma, a European-based company he founded in 2009 that is focused on the research of rare and neglected diseases. Noventia Pharma operates in Southern Europe, and offers a product portfolio of pharmaceuticals with a specialized business dedicated to treatments of rare and neglected diseases. Massimo also serves as Executive Chairman of Bioakos Pharma, a specialty pharmaceutical company based in Florence, Italy, and focused in the areas of dermatology, gynecology and pediatrics. Before Noventia, Massimo served as the President and C.E.O. of Dompe International, where he spearheaded the company’s global growth in over 65 nations worldwide. Massimo holds a Ph.D. from the University of Milan, where he graduated with honors, and currently serves on the boards of various companies such as Bioakos Pharma, Arriani International and Ariad Pharmaceuticals. He also serves as an advisor for the Irish Government Enterprise Ireland and the Health Commission of the Senate of Italian Republic for Rare and Neglected Diseases.

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MichelDeWilde200MICHEL DEWILDE, PHD

Michel De Wilde joined the IDRI Board of Directors in October 2014. Currently serving as a consultant for the international vaccine community, Michel De Wilde was among the first to use recombinant DNA technology in the industry and has contributed to the discovery and development of a number of vaccines.

From 2001 through 2013, De Wilde was Senior Vice President, Research & Development, at Sanofi Pasteur, the human vaccines division of Sanofi, where he supervised a broad portfolio of discovery and development projects, including the first Dengue vaccine that recently successfully completed phase 3 During his tenure at Sanofi Pasteur, De Wilde drove the development and licensure by the U.S. Food and Drug Administration of a number of products, including the first tetravalent meningococcal conjugate, the first prototype H5 pandemic vaccine and the first intradermal influenza vaccine, Intanza, which was also licensed by the European Medicines Agency. He also oversaw the licensure, under accelerated approval, of a new high-dose formulation of an influenza vaccine, which demonstrated superior efficacy to conventional vaccines in clinical trials. De Wilde was also instrumental in driving the acquisition of and defining the integration model for two biotech companies, Acambis and VaxDesign.

Prior to joining Sanofi Pasteur, De Wilde was at SmithKline Beecham Biologicals (now GSK Vaccines) in Belgium. He joined the group in 1978 as a research scientist and subsequently held positions of increasing responsibility to become Vice President, Research & Development, heading a team active in all aspects of preclinical vaccine development.

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ChrisHentschelCHRIS HENTSCHEL, PHD

Chris Hentschel has served on IDRI’s Board of Directors since March of 2010. He is a Founder, former Chief Executive Officer, and Board member of the Medicines for Malaria Venture (MMV), a nonprofit Geneva-based Swiss Foundation. MMV operates as a public/private partnership which, with its pharmaceutical partners, funds and manages the World's largest portfolio of anti-malarial drug discovery and development projects. Prior to joining MMV, Chris acted as Senior Vice President and Chief Scientific Officer of Centocor, Inc. where he was responsible for all aspects of technology strategy and the development of the product pipeline. From 1978 to 1997, Chris was Chief Executive Officer and Scientific Director of the UK Medical Research Council's Collaborative Centre (now renamed MRC Technology), where he managed more than forty industrial drug discovery and development collaborations with both global pharma and biotechnology companies. Chris started his career at Celltech Ltd., Europe's largest biotechnology company, during the company’s start-up phase. He was Head of the Department of Molecular Genetics and helped set up the company’s R&D operations. Currently, Chris serves on the boards of the Global Medical Forum Foundation (GMF, Zurich) and MSM Protein technologies. He is also a partner of Life Science Ventures (LSV, Cayman Islands).

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lFRANKLYN G. PRENDERGAST, MD, PHD

Franklyn Prendergast has served on IDRI's Board of Directors since October of 1999. He is the Edmond and Marion Guggenheim Professor of Biochemistry and Molecular Biology and Professor of Molecular Pharmacology and Experimental Therapeutics at the Mayo Medical School. In the past, he has served as the Director of the Mayo Clinic Cancer Center and Director of the Mayo Clinic Center for Individualized Medicine and as the Chair of the Department of Biochemistry and Molecular Biology at the Mayo Clinic. He has also served on the Board of Trustees and on the Board of Governors of the Mayo Foundation. Franklyn's research focuses on structural protein biology and bioimaging and has earned him numerous honors, including an E.E. Just Award from the American Society of Experimental Biology and the Musgrave Gold Medal of the Institute of Jamaica. As a Rhodes Scholar, Franklyn earned his BA and his MA from Oxford University. He then went on to receive his MD from the University of the West Indies, and his PhD from the University of Minnesota. He has also received honorary DSc's from Purdue University and the University of the West Indies.

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bio-gail-cassellGAIL CASSELL, PHD

Gail H. Cassell, Vice President of TB Drug Development, IDRI, is also a Visiting Professor in the Department of Global Health and Social Medicine at Harvard Medical School. Gail recently retired as Vice President, Scientific Affairs and Distinguished Lilly Research Scholar for Infectious Diseases at Eli Lilly and Company in Indianapolis where she was responsible for launching the Lilly MDR-TB philanthropic effort and establishing and leading the Lilly TB Drug Discovery Initiative, a nonprofit launched in 2007. Formerly she was Vice President of Infectious Diseases Drug Discovery and Clinical Development at Lilly, where she led a hepatitis C protease inhibitor program from the discovery phase to clinical candidate, and the development of a new antibiotic from clinical development to product decision. Prior to Lilly, Gail served as the Charles H. McCauley Professor and Chairman of the Department of Microbiology at the University of Alabama Schools of Medicine and Dentistry at Birmingham.

Gail has served on a number of boards and committees, and is currently a member of the NIH Science Management Board, the newly appointed NIH Board of Trustees, and the Advisory Council of the Fogarty International Center of NIH. A member of the Institute of Medicine of the National Academy of Sciences, Gail has been widely recognized for her research accomplishments including two honorary degrees.

Gail received her BS from the University of Alabama in Tuscaloosa and obtained her PhD in Microbiology from the University of Alabama at Birmingham.

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©Earl HarperERIK IVERSON, JD, LLM

President, Business & Operations

Erik Iverson is the President, Business & Operations at IDRI. Prior to joining IDRI, Erik was Associate General Counsel at the Bill & Melinda Gates Foundation, where he was the second attorney on staff and worked for over seven years exclusively within the Foundation's Global Health Program, where he led the development and implementation of the foundation's Global Access policy through the review of grant proposals and assistance in structuring strategic initiatives. More particularly, Erik worked closely with foundation staff and grantees in the development of intellectual property management and collaboration agreements, novel financing arrangements, and product development and "global access" strategies. Previously, Erik was an attorney at the law firm of Perkins Coie LLP, where he represented life science companies in the negotiation of financing transactions, joint ventures, research collaborations, licensing arrangements, and manufacturing agreements. Erik received his JD from the University Of North Dakota School Of Law in 1994 and his Masters of Law (LLM) in Taxation from New York University School of Law in 1995.

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Antony-Profile200CHRISTOPHER ANTONY

Vice President, Operations & Environmental Health & Safety Officer

Chris Antony is the Vice President of Operations at IDRI and also serves as IDRI’s Environmental Health and Safety Officer. In addition, Chris acts as administrator to IDRI's Institutional Biosafety Committee and serves as a member of the organization's FISMA Joint Authorization Board. As VP of Operations, Chris has oversight of several functional areas including facilities, information technology and quality control.

Chris joined IDRI in 2011 as Facilities Manager after spending more than 35 years in private industry, most recently with a Washington-based OTC drug manufacturer and provider of safety services.

Chris graduated from the University of California, Berkeley, with a degree in Political Science.

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Beckmann-Profile200ANNA MARIE BECKMANN, PHD

Senior Vice President, Product Development & Regulatory Affairs

Anna Marie Beckmann is the Vice President of Product Development and Regulatory Affairs at IDRI. She is responsible for guiding products through the transitional phase from pre-clinical research to evaluation in clinical trials. In the regulatory affairs arena, her group provides the necessary documentation to the U.S. Food and Drug Administration for review and approval of IDRI's vaccine and adjuvant candidates in human clinical trials. She is also responsible for IDRI's in-house pilot manufacturing facility that produces cGMP adjuvant formulations for Phase 1 vaccine clinical trials.
Anna Marie was a Senior Fellow in the STD Training Program at the University of Washington and a faculty member at the Fred Hutchinson Cancer Research Center, where her research focused on the pathogenesis of human papillomavirus infections (HPV) and the relationship between HPV infections and human anogenital cancers. In 1998 she joined Corixa Corporation as Director of Regulatory Affairs and worked on early stage clinical development of vaccines for infectious diseases and cancer.

Anna Marie Beckmann earned her PhD from the Department of Immunology and Infectious Diseases at Johns Hopkins University School of Public Health. Her thesis was focused on the pathobiology of infection with the human papillomaviruses JC and BK.

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Dan Stinchcomb 200DAN STINCHCOMB, PHD

Senior Vice President, Vaccine Development & Viral Disease Programs

Dan Stinchcomb is the Sr. Vice President for Vaccine Development and Viral Disease Programs at IDRI. He began his career in assistant and associate professor roles at Harvard and then moved to senior scientific leadership positions at Synergen Inc. and later Ribozyme Pharmaceuticals Inc., where he served as Director of Biology Research. He then moved into the field of veterinary products at Heska Corp., where he led all aspects of product research and development. In 2005, Dan co-founded and served as President and CEO of Inviragen Inc., which he transformed from a virtual start-up to a global clinical stage company with sites in Colorado, Wisconsin and Singapore and translated two vaccines from the research bench to human clinical trials, including one for dengue fever. In 2013, Inviragen was acquired by Takeda Pharmaceutical Company Limited. Dan also serves as Executive Chair of FluGen, Inc., a biotechnology company developing a novel, single round replicating influenza vaccine.

Dan has authored over 50 scientific publications, is an inventor on more than 30 patents and serves as a member of the Vaccines Policy Advisory Committee for BIO, the world’s largest biotechnology trade association. Dan received his PhD from Stanford University and his BA from Harvard College.

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Doug Bradley 200R. DOUGLAS BRADLEY, PhD, JD

General Counsel & Secretary

Doug Bradley is the General Counsel and Secretary at IDRI. Prior to joining IDRI, Doug was Vice President & Intellectual Property Counsel at Unigen, Inc., a privately held, natural products discovery company. Previously, Doug was Assistant Counsel for Patent and Corporate Development & Licensing at Merck and Co., Inc.’s affiliate company, Rosetta Inpharmatics. Doug is experienced in all phases of intellectual property and licensing/contract law, in particular, negotiating and drafting of intellectual property licensing agreements, collaboration agreements, clinical trial agreements, supply and manufacturing agreements, and many other corporate agreements, intellectual property due diligence, strategic management of patent portfolios, patent application preparation and prosecution, and patent opinion work. Doug is admitted to the Washington State Bar Association and is a registered patent attorney with the United States Patent and Trademark Office.

Doug received his PhD in molecular, cellular and developmental biology from the University of Colorado at Boulder, and did postdoctoral research in plant genetic engineering at the Plant Breeding Institute in Cambridge England. Doug received his JD (with honors) from the University of Washington. Prior to going to law school, Doug was a Research Assistant Professor at the University of Washington in the Department of Botany.

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Carter-Profile200DARRICK CARTER, PHD

Vice President, Adjuvant Techology

Darrick Carter is the Vice President of Adjuvant Technology at IDRI. His work centers on new immunomodulatory agents and formulations, as well as the process development necessary to take vaccines and therapeutic candidates from the lab to the clinic.

Darrick is a biochemist/biophysicist with over 15 years of experience developing therapeutics and vaccines in the biotechnology industry. He has founded five companies, starting with a sole proprietorship biotech/internet startup, Proteinchemist.com, in 2001. Darrick previously worked at Corixa Corporation, where he led a new tuberculosis vaccine into human clinical trials and assisted as group leader for analytical biochemistry working on adjuvants and a commercial, radiolabeled mAb for non-Hodgkins lymphoma.

In 2004, he founded and served as CEO of PAI Life Sciences Inc., a bioinformatics company with proprietary drug discovery technologies using artificial neural nets. Darrick also served as Chief Scientific Officer at a specialty pharmaceutical company focused on drug and device combinations, is a founding member of a company focused on immunotherapy in oncology, and a founding member of a device company working on inflammatory disorders. Darrick sits on the Scientific Advisory Boards of three local biotech companies and hosts a website for protein chemists. He has authored over 50 peer-reviewed papers and is inventor/co-inventor on more than 160 patent applications and issued patents.

Darrick received his BSc summa cum laude from the department of Biochemistry and Biophysics at Oregon State University. He received his PhD from the Department of Biochemistry and Molecular Biology at Oregon Health and Science University.

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Coler-Profile200RHEA COLER, PHD

Senior Vice President, Pre-clinical & Translational Science

Rhea Coler is the Vice President of Preclinical Biology at IDRI. Her work focuses on the characterization of candidate vaccines for tuberculosis, leishmaniasis, pneumococcus, malaria and chlamydia. Uncovering the roles that innate and adaptive immunity play during these infectious processes are key research questions in the Coler lab. Elucidating the mechanisms of protection against these diseases could lead to the development of novel prophylactic and therapeutic interventions.

Rhea currently serves on the boards of the SPHCM and Bertschi School, and is an Affiliate Associate Professor in the Department of Global Health at the University of Washington. She has been the recipient of several fellowships and grants awarded by the NIH/NIAID, the Medical Research Council (MRC), and PATH Vaccine Solutions. She has several patents and has co-authored more than 20 original articles. After doing field work on malaria control in Tanzania, she returned to Trinidad where she worked in the Department of Parasitology and Entomology at the Caribbean Epidemiology Center (CAREC), funded in part by the Center for Disease Control and the World Health Organization.

Rhea received her BSc from McGill University and her MSc in the field of Medical Parasitology at the London School of Hygiene and Tropical Medicine. She obtained her PhD from the School of Public Health and Community Medicine (SPHCM) at the University of Washington.

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Fox-Profile200CHRISTOPHER FOX, PHD

Vice President, Formulation / Principal Investigator

Since joining IDRI in 2007, Chris has played an integral role in developing, characterizing, and manufacturing cGMP vaccine adjuvant formulations for a variety of infectious diseases, including leishmaniasis, malaria, tuberculosis, pandemic influenza, and amebiasis, resulting >40 publications. He currently serves as principal investigator on a $11.9M contract from the National Institutes of Health (NIH) to develop a thermostable tuberculosis vaccine suitable for distribution in developing countries, involving formulation development, cGMP manufacturing, and clinical testing.

From 2010-2014, he led a $1.4M BARDA-funded effort to transfer adjuvant manufacturing technology to the Cantacuzino Institute in Bucharest, Romania. He has also participated in technology transfer projects in Brazil and India, where a vaccine formulation center has been constructed to manufacture IDRI-developed adjuvant formulations for clinical trials to evaluate malaria, leishmania, and tuberculosis vaccines.

Besides his current appointment as an Assistant Affiliate professor in UW’s Department of Global Health, Chris’s educational outreach activities include serving as a faculty member for the Advanced Vaccinology Course in India (2010-2014) and for the online Spanish-language Latin American Diploma on Vaccinology sponsored by the Carlos Slim Health Institute. Finally, he serves as Associate Editor of the journal Therapeutic Advances in Vaccines published by SAGE. Chris obtained his Ph.D. in Bioengineering at the University of Utah and his B.S. at Utah State University.

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Parish-Profile200TANYA PARISH, PHD

Vice President, Drug Discovery

Tanya Parish is the Vice President of Drug Discovery at IDRI where she heads the TB Discovery Research group. Her work focuses on the discovery of new drugs that are effective at curing drug-sensitive and drug-resistant tuberculosis with the added goal of shortening the time it takes to cure disease. This encompasses a range of early stage drug discovery including drug target identification and validation, high throughput screening and medicinal chemistry. In addition, her group works to understand the pathogenic mechanisms and basic biology of the global pathogen Mycobacterium tuberculosis and using this information to inform drug discovery.

Tanya is a microbiologist by training, with a background in mycobacteriology. She received her PhD at the National Institute for Medical Research investigating gene regulation in mycobacteria followed by postdoctoral research at the London School of Hygiene & Tropical Medicine studying several facets of the biology of M. tuberculosis. Until recently, she held an academic post as Professor of Mycobacteriology at Barts and the London School of Medicine and Dentistry, and she is currently an Affiliate Professor in the Department of Global Health at the University of Washington.

Tanya has edited several books on mycobacteria and published numerous papers on the basic biology and genetics of M. tuberculosis. She is
Editor-in-Chief of Microbiology (UK), on the Editorial Board for PLOS One, PeerJ and Frontiers in Cell and Infection Microbiology.

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Lin-Profile200ROB LIN, PHD, CFA

Vice President, Finance

Rob Lin is Vice President of Finance at IDRI where he brings a passion for healthcare issues to the fiscal and strategic management of IDRI. Previously, Dr. Lin was Deputy Director in Financial Planning & Analysis at the Bill & Melinda Gates Foundation. Prior to that, he worked in Corporate Development at Millennium Pharmaceuticals and as a Senior Consultant with Dean & Company Strategy Consultants. He earned a Ph.D. in Human Genetics at Harvard University. Dr. Lin is a CFA charter holder as well as a term member of the Council on Foreign Relations.

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Wicomb-Profile200WINSTON WICOMB, PHD, LATG

Director, Vivarium

Winston Wicomb is the director of all animal studies and serves as chair of the Institutional Animal Care and Use Committee (IACUC) at IDRI. He is also the manager of the vivarium staff. Winston is a biochemist with over 20 years of experience in biochemistry and transplantation research in the fields of heart, liver, and kidney preservation. Winston also served on the team that flew the first human heart for transplantation using continuous hypothermic perfusion. To date, he has over 60 publications on his work in heart, kidney and liver preservation.

Prior to joining IDRI, Winston supervised the laboratories of the late Christian Barnard in South Africa, and Dr. G. Collins at the California Pacific Medical Center in San Francisco. Winston has served as the lead biochemist involved in chemical processing of porcine and bovine tissues for clinical transplantation. He has a broad knowledge of animal care, and chaired three IACUC committees since the early 1990s..

Winston received his Ph.D. in Medical Biochemistry from Cape Town University in South Africa.

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bio-thomas-vedvickTHOMAS VEDVICK, PHD

Vice President, Formulation and Process Development

Thomas Vedvick is the Vice President of Formulation and Process Development at IDRI. Tom's research interests are focused on the development of large scale protein purification and the characterization of proteins for vaccine development. In addition, Tom directs the exciting adjuvant formulation program at IDRI. He has more than 70 original articles, and holds 28 issued U.S. patents for diagnostics, vaccines, and therapeutics of infectious diseases and cancer.

Prior to joining IDRI, Tom worked at the Salk Institute Biotechnology Industrial Associates (SIBIA) where he led the protein purification and characterization laboratory. While at SIBIA he collaborated on the development of the Pichia pastoris recombinant protein expression system. Tom later left SIBIA to work at Telios Pharmaceuticals, where he developed peptide based products for wound healing. Tom then joined Corixa Corporation where he established a protein microsequencing facility and directed the process development group which focused on vaccines for infectious diseases and cancer. Afterwards, Tom spent two years working at LigoCyte pharmaceuticals, where he served as Director of Process Development and Project Leader in the Norovirus vaccine program. He led the development of purification methods, formulation, and cGMP contract manufacturing of the Norovirus,Virus Like Particles. This successful program was the first product that reached a phase I clinical trial for LigoCyte Pharmaceutical.

Tom obtained his BSc in Chemistry from the University of Puget Sound, his MSc in Chemistry from Western Washington State University, and his PhD in Biochemistry from Oregon Health Sciences University.

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bio-susan-baldwinSUSAN BALDWIN, PHD

Senior Scientist / Principal Investigator

Susan Baldwin is a Senior Scientist and Principal Investigator at IDRI. Dr. Baldwin has been at IDRI for over six years and currently works on projects related to development of next-generation vaccines against infectious diseases. Her research involves preclinical immunology and efficacy of vaccines against H5N1 pandemic influenza, malaria, and Mycobacterium tuberculosis using mouse, ferret and guinea pig models.

One of the pandemic influenza projects Susan focuses on is development of an effective virus like particle (VLP) vaccine given intradermally, using microneedle technology. The other two pandemic influenza projects focus on the efficacy of recombinant protein and VLP pandemic influenza vaccines combined with IDRI’s adjuvant technology. Similar to these projects, IDRI’s subunit tuberculosis vaccine, ID93, also utilizes adjuvants that induce a cell-mediated immune response, which is required for protection against M. tuberculosis infection in low dose aerosol models of TB.

Susan received her PhD in Microbiology and Immunology at Colorado State University in Fort Collins. She completed her doctorate work in Dr. Ian Orme’s laboratory where she focused on the development of several novel vaccines against M. tuberculosis.

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Korkegian-Profile200AARON KORKEGIAN, PHD

Scientist I

Aaron Korkegian is a Scientist with the TB Drug Discovery team at IDRI. Aaron’s work involves the management of projects and assays involved in drug discovery for tuberculosis. His work currently focuses on biological assay development, management of high throughput screening and the progression of compound series in a highly collaborative effort. His previous work at IDRI has included investigations into the physiology of the M.tuberculosis (Mtb) cell wall, the development of an overexpression library for high throughput target identification, and the development of target based high throughput screens for potential drug candidates against Mtb.

Aaron received his BSc in Molecular Biology from Pomona College and his Ph.D. in Molecular and Cellular Biology from the University of Washington. His graduate work at the Fred Hutchinson Cancer Research Center focused on protein biochemistry and engineering with work culminating in the first example of successful thermostabilization of an enzyme using computational design techniques.

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Jee-Profile200JO-ANN JEE, PHD

Postdoctoral Scientist

Jo-Ann Jee is a Postdoctoral Scientist in the TB Drug Discovery Group. Her work focuses on the design, synthesis, and development of novel agents for the treatment of tuberculosis.

Jo-Ann received a BSc in Biochemistry from Trinity College and her PhD in Chemistry from Stony Brook University. Her graduate research, under the mentorship of Dr. Jonathan G. Rudick, focused on the convergent synthesis of dendrimers via isocyanide multicomponent reactions.

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Hsu-Profile200FAN-CHI HSU, PHD

Postdoctoral Scientist

Fan-Chi Hsu is a Postdoctoral Scientist in Preclinical group at IDRI. Her work focuses on using RNA vaccines for Leishmaniasis and prostate cancer to generate protective or therapeutic immune responses in mouse models and evaluate in an artificial lymph node system. She also investigates the cellular and molecular mechanisms of innate and adaptive immune responses by RNA vaccines.

Fan-Chi received her bachelor and master degree in field of allergic immunology from National Taiwan University in Taiwan. She earned her PhD in immunology from Mayo Graduate School of Mayo Clinic in Minnesota. Her doctoral work with Dr. Virginia Smith Shapiro focused on elucidating the role of transcription regulators (NKAP, HDAC3 and Runx1) in T cell maturation using conditional knockout mouse models and multi-color flow cytometry, and identifying novel mechanisms such as complement and sialylation that monitor the maturity of recent thymic emigrants.

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Howell-Profile200HEATHER HOWELL, PHD

Postdoctoral Scientist

Heather Howell is a Postdoctoral Scientist in the TB Drug Discovery group at IDRI. Her work focuses on identifying and validating protein targets of small molecules capable of killing Mycobacterium tuberculosis.

Heather received a BA in Biochemistry from Hood College in Frederick, MD, and a MS in Biotechnology from Johns Hopkins University. She went on to earn a PhD under the mentorship of Dr. Alan Hauser in the department of Microbiology-Immunology at Northwestern University. Her thesis work focused on furthering understanding of the role of the type III secreted toxin ExoU to the pathogenesis of acute Pseudomonas aeruginosa pneumonia.

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Fedor-Profile200DAWN FADOR, PHD

Postdoctoral Scientist

Dawn Fedor is a Postdoctoral Scientist in the Characterization and Product Development Group. Dawn’s work focuses on developing analytical methods to support further characterization of vaccine antigen and adjuvant components, as well as vaccine formulation development.

Dawn received her BS in Nutritional Sciences from Rutgers University and her PhD in Nutritional Biochemistry with a Designated Emphasis in Biotechnology from University of California, Davis. Her graduate work focused on using analytical biochemistry to elucidate the role of omega-3 fatty acids in the prevention and reversal of non-alcoholic fatty liver disease. Following graduate school, she completed an internship at BioMarin Pharmaceutical between the Process Development and Analytical Chemistry Groups and worked as a Postdoctoral Researcher at University of California, Berkeley.

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Day-Profile200TRACEY DAY, PHD

Scientist I

Tracey Day is an immunologist in the Clinical Immunology group. Tracey’s research interests include:

  • Developing novel and much needed vaccines for infectious diseases including tuberculosis and leishmaniasis.
  • Evaluating immunogenicity and efficacy of candidate vaccines in clinical trials.
  • Investigating immune responses correlating with protection from infection.

Tracey received her Ph.D. working with Dr. Stefan Kaufmann at the Max Planck Institute for Infection Biology in Berlin, Germany. Her doctoral research focused on the pulmonary immune responses elicited during tuberculosis. Tracey completed postdoctoral research with Dr. David Sherman at the Center for Infectious Disease Research in Seattle, WA. Her studies there focused on investigating host-pathogen interactions between Mycobacterium tuberculosisand pulmonary immune cells during the early stages of infection. Before joining IDRI, Tracey worked as a Protocol Development Manager with the HIV Vaccine Trials Network at the Fred Hutchinson Cancer Research Center where she led multi-disciplinary teams in the design and implementation of clinical trials evaluating candidate HIV and tuberculosis vaccines.

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Manning-Profile200ALYSSA MANNING, PHD

Scientist I

Alyssa Manning is a Scientist I in the TB Drug Discovery group at IDRI. Alyssa’s work involves developing new high content assays for drug and adjuvant screening. She is currently focusing on M. tuberculosis drug screening in mammalian macrophages infected with the bacteria. This fluorescence-based assay will allow for simultaneous determination of potential drug efficacy towardM. tuberculosis and cytotoxicity toward macrophages in a high throughput manner.

Alyssa’s previous scientific endeavors focused on embryonic cell biology in model organisms and development of novel image analysis techniques. She received her BA in Biology from Pomona College and worked there as a laboratory technician after graduation. Alyssa’s Ph.D. work at the University of North Carolina at Chapel Hill included elucidation of signaling pathway components necessary for gastrulation in Drosophila. As a postdoctoral fellow at the University of Washington she developed a method to image and track cell migration in live zebrafish embryonic tissue explants.

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Laursen-Profile200ERIK D. LAURSEN

Director, GMP Operations

Erik is a biopharmaceutical development and operational professional with more than 20 years of drug development, project management and manufacturing/operational experience in pharmaceutical and biotechnology companies in North America and Europe. His experience includes extensive time spent in business development; with in/out licensing; and in the purchase/sale of CMO [Contract Manufacturing Organization] services.

At IDRI, Erik is the Director, GMP (Good Manufacturing Practice) Operations. Previous to IDRI, he was with CMC Biologics from 2005-2010 and at NeoRx, Seattle, for the preceding 5 years as Sr. Director, Manufacturing, and Director of Operations with responsibilities for radio pharmaceutical production, biopharmaceutical pilot manufacturing and contract manufacturing activities. Previously Erik held leadership positions in development and operations at ZymoGenetics in Seattle. He received his MS in Biochemical Engineering from the Technical University of Denmark.

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Kumar-Profile200ANURADHA KUMAR, PHD

Scientist I

Anu is a Scientist in the TB Discovery Research group at IDRI. She works in a team exploring new molecules to treat tuberculosis; specifically she is developing tools to help prioritize molecules as they progress through the early stages of the discovery pipeline.

Anu first moved to the USA from India to attend Bard College, in upstate New York. After completing her B.A. she went on to study Biochemistry and received her PhD from Tufts University. She moved to the West Coast for her Postdoctoral research and worked with David Sherman at Center for Infectious Disease Research, where she gained experience working with M. tuberculosisand also developed and ran high throughput biochemical screens and target-based whole-cell screens. She worked as an Open Lab Fellow at GSK’s Tres Cantos Laboratories working on both whole-cell and biochemical screens. Most recently she was a Scientist at Open Source Drug Discovery, a unit of the Indian Government, dedicated to developing and strengthening the contributions of Indian institutes to the entire tuberculosis drug discovery pipeline. She returned to Seattle in 2015 and joined IDRI where she is excited about continuing to contribute to the global efforts to find better drugs to treat tuberculosis.

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RyanKramerRYAN KRAMER, PHD

Senior Scientist

Ryan Kramer is a Senior Scientist at IDRI and Manager of the Characterization and Product Development group. Ryan is responsible for characterization of vaccine antigen and adjuvant components and for vaccine formulation development to achieve thermostable products that do not depend on the cold-chain for distribution to developing countries. Ryan has worked in a wide range of disease fields including cancer, HIV, tuberculosis, leishmaniasis, anthrax, West Nile virus, leprosy, hookworm disease, schistosomiasis, chikungunya virus, and shigellosis.

Before joining IDRI, Ryan was a postdoctoral fellow at the Macromolecule and Vaccine Stabilization at the University of Kansas, under the supervision of Russ Middaugh and David Volkin. He worked on over 12 contract and research formulation development projects characterizing different macromolecular systems and biotherapeutics, using state of the art analytical biophysical instrumentation.

Ryan obtained his Ph.D. in biochemistry from Texas A&M University where he developed a mutational approach for increasing protein solubility. As a graduate student, Ryan received a Molecular Biophysics NIH predoctoral training grant and Texas A&M Regents' Graduate Fellowship. He served as Vice President of the Biochemistry Graduate Student Association and organized the 18th annual Biochemistry and Biophysics research competition.

Ryan graduated summa cum laude from Washington State University and received his B.S. in biochemistry. Ryan is an Eagle Scout and member of Order of the Arrow.

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Vanhoeven-Profile200NEAL VAN HOEVEN, PHD

Senior Scientist

Neal Van Hoeven is a Senior Scientist at IDRI. Neal’s work is focused on pre-clinical downselection and evaluation of vaccine adjuvants for several emerging viral diseases. His ongoing research projects include programs to develop adjuvants for use with H5N1 pandemic influenza antigens as well as West Nile Virus vaccines. In addition, he is interested in understanding the effect that adjuvants have on the generation and maturation of antiviral antibodies, and is working to develop a number of high-throughput techniques for evaluation of complex antibody responses following vaccination in animals and humans.

Prior to joining IDRI, Neal worked as a research scientist for Immune Design Corporation (IDC), where he was a member of a team focused on design, generation, and testing of a novel viral vector vaccine platform.

Neal received his Ph.D. from the Molecular and Cellular Biology program at the University of Washington in 2005, where he worked in the laboratory of Dr. Dusty Miller, focusing on development of new viral vectors for use in gene therapy. He carried out his post-doctoral studies in the Influenza Division at the Centers for Disease Control and Prevention (CDC) in Atlanta under the supervision of Dr. Terrence Tumpey and Dr. Jacqueline Katz, where he worked to understand transmissibility of highly pathogenic influenza viruses.

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Aude Frevol 200AUDE FREVOL, RN, PMP

Clinical Trial Manager

Aude is a Clinical Trial Manager in the Clinical team. Her role includes project management and clinical trial management to support the development of IDRI’s vaccine candidates. She contributed to the success of the recent clinical trials conducted in the U.S., Sudan, Peru and South Africa. She started her career in the pharmaceutical industry in the early 90s, working at Astra, then Aventis in Paris, France, for the clinical development of respiratory and allergic diseases compounds.

Prior to that, she held various positions as a registered nurse in the ward including volunteering in rural India in a leprosy center. A native from Lyon, France, she earns a Nursing Degree (RN) and is a certified Project Management Professional (PMP).

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EduardMeliefProfileEDUARD MELIEF, PHD

Postdoctoral Scientist

Eduard Melief is a Postdoctoral Scientist in the TB Drug Discovery group at IDRI. His work focuses on drug target identification and validation for the pathogen Mycobacterium tuberculosis. He is using a variety of approaches to measure drug-protein interactions, and identify the bacterial protein targets of new anti-tubercular drugs in development.

Eduard earned his BA in Biochemistry and Molecular Biology from Franklin & Marshall College and his PhD in Biochemistry and Structural Biology from Stony Brook University. His doctoral work with Dr. Peter J. Tonge focused on elucidating the mechanism of GFP chromophore maturation using protein semi-synthesis. He went on to a postdoctoral position with Dr. Iwao Ojima evaluating anti-tubercular compound series that inhibit the cell division protein FtsZ and screening computationally designed small molecule inhibitors of Botulinum neurotoxin.

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Odingo-Profile200JOSHUA OLUOCH ODINGO, PHD

Director, Chemistry

Joshua Odingo is the Director of Chemistry in the TB Drug Discovery Group. Joshua is an organic/medicinal chemist with many years of experience in small-molecule drug discovery. His work focuses on the application of medicinal chemistry to the development of novel agents for the treatment of tuberculosis. He is also working on tool molecules for target identification and interrogating disease biology.

Prior to joining IDRI, Joshua was a Senior Staff Scientist and a chemistry group leader at ICOS Corporation. He received his B.Sc. in chemistry from Nairobi University and a Ph.D. in organic chemistry from Columbia University, followed by a postdoctoral fellowship at Genentech Incorporation.

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OrrM-Profile200MARK ORR, PHD

Senior Scientist / Principal Investigator

Mark Orr, Ph.D. is an immunologist in the Pre-Clinical Biology group. As a Senior Scientist and Principal Investigator at IDRI his research interests include:

  • Developing novel adjuvanted vaccines for bacterial diseases including tuberculosis that have a major impact on global health.
  • The cellular and molecular mechanisms of adjuvant activity.
  • Immunologic characterization and development of new vaccine adjuvants.

Mark is also an Affiliate Assistant Professor in the University of Washington, Department of Global Health Interdisciplinary Pathobiology Program. He has published over 25 peer-reviewed articles in the fields of immunology and vaccine development. He is a member of the American Association of Immunologists and serves on the editorial board of Frontiers in NK Cell Biology.

Mark received his Ph.D. from the Department of Immunology at the University of Washington. His thesis work with Dr. Chris Wilson was focused on the immune evasion strategies employed by herpes simplex virus. Mark did his postdoctoral work with Dr. Lewis Lanier at the University of California, San Francisco, where he researched the response of natural killer (NK) cells to viral infection, studying both the signaling pathways and educational programs that shape NK cell responses to infection in vivo.

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Chettiar-Profile200SOMSUNDARAM CHATTIAR, PHD

Postdoctoral Scientist

Somsundaram N. Chettiar is a Postdoctoral Scientist in the TB Discovery Research group at IDRI. His work focuses on the development of novel small molecules for the treatment of tuberculosis.

Somsundaram received a BS in Pharmaceutical Sciences from University of Mumbai, India, and a MS in Pharmacy from University Department of Chemical Technology, India. He went on to earn a PhD under the mentorship of Dr. Pui-kai Li and Dr. Chenglong Li from the College of Pharmacy at the Ohio State University. His thesis work focused on developing novel small molecule inhibitors against protein targets such as survivin and STAT3 that are essential for progression and survival of cancer.

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bio-julie-earlyJULIE EARLY, PHD

Scientist I

Julie Early is a Scientist I in the TB Drug Discovery Group. Julie's work involves several aspects of early stages of drug discovery for tuberculosis. Her work focusses on microbiological aspects including assay development, high throughput screening, and progression of compound series using numerous biological techniques to profile compounds. She is also involved in identifying the mechanism of action of anti-tubercular compounds.

Julie received her BSc in cell biology from St. Cloud State University. She received her Ph.D. from Oregon State University, where her thesis work involved the characterization of the intracellular phenotype of Mycobacterium avium. After a brief time working on the lvh type IV secretion system of Legionella pneumophila, she returned to studying Mycobacteria. She appreciates that her work at IDRI is applied and will lead to an improvement in the lives of tuberculosis patients in the future.

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Bonnett-Profile200SHILAH BONNET, PHD

Scientist I

Shilah Bonnett is a Scientist I in the TB Drug Discovery group at IDRI. Shilah's work focuses on the development of target based high throughput screens to identify potential drug candidates for the treatment of tuberculosis.

Shilah received her BSc in Environmental Science/Toxicology from Western Washington University and her PhD in Chemistry from Portland State University. Her graduate research focused on the enzymology of tRNA modification in bacteria. Prior to joining IDRI in 2013, Shilah worked at Portland State University as a Postdoctoral Scientist studying the metabolic pathways and enzymes involved in the generation of natural products (drug discovery) and olefins (biofuels development).

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Ovechkana200YULIA OVECHKINA, PHD

Director, High Throughput Screening

Yulia Ovechkina is the Director of High Throughput Screening for the Tuberculosis Discovery Research Group at IDRI. Her work is focused on maintaining existing and developing new screening assays and automated workflows as well as data analysis and database management.

Yulia has an extensive expertise in the assay development, assay miniaturization, high throughput screening (HTS), automation and data analysis. Previously, she developed an innovative High Content Screening HTS platform, OncoPanel, to profile therapeutic cancer agents across 240 human tumor cell lines at Ricerca Biosciences (formerly MDS Pharma Services). Prior to joining Ricerca Biosciences, she developed in vitro cellular immunology assays as a postdoctoral research fellow at Children's Hospital and Regional Medical Center, Department of Immunology in Seattle, WA. Yulia earned Ph.D. in Physiology and Biophysics from the University of Washington and M.S. in Molecular Genetics from the Ohio State University. She received B.S. in Cytology and Genetics from the Novosibirsk State University in Russia. She has authored or co-authored more than 12 peer-reviewed publications and is a member of the editorial advisory board of the Combinational and High Throughput Screening (CCHTS) journal.

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Patel-Profile200NIPUL PATEL, PHD

Postdoctoral Scientist

Nipul Patel is a Postdoctoral Scientist in TB Discovery Research group at IDRI. His research focuses on the identification and validation of mycobacterial proteins as drug targets, and elucidating mechanism of action of drugs active against Mycobacteria.

Nipul received his PhD at St. John’s University, New York. His doctoral research was focus on elucidating mitochondrial fission pathway in the human parasite Leishmania, to develop new therapeutic interventions. He received his MS in Zoology, specialization in Human Biology and reproductive physiology in India, as well as a BS with honors in Zoology.

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Duthie-Profile200MALCOLM DUTHIE, PHD

Senior Scientist

Malcolm Duthie is a Senior Scientist at IDRI. Malcolm's main research interest lies in determining and examining the host/pathogen interactions that initiate and control immune responses, how these interactions can be beneficially manipulated, and, ultimately, their practical application within disease control programs.

Malcolm received his training through a BSc (Hons) Immunology from the University of Glasgow, Scotland, and a Ph.D. in Medical Microbiology from the University of Edinburgh, Scotland. He then conducted postdoctoral work at the University of Washington where he examined protective and pathologic immune responses during experimental T. cruzi infection. He now works with an extensive network of collaborators in several countries to identify vaccine candidates and develop new diagnostic tools to improve the control of neglected tropical diseases, with particular focus on leprosy and leishmaniasis.

Malcolm is currently an Affiliate Assistant Professor, Department of Global Health, University of Washington School of Medicine, Seattle; a Visiting Professor to the CAPES-Fiocruz/CDTS long-term collaboration program in Brazil; and a Foreign Expert Consultant to Center for Major Infectious Disease, Capital Medical University, Beijing, China. Malcolm serves as a member of the Editorial Boards of Infection and Immunity (2012-17) and Journal of Advances in Diseases Diagnosis (2014-) and is a member of the American Association of Immunologists, American Society for Microbiology and American Society of Tropical Medicine and Hygiene, and British Society for Immunology.

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Roberts-Profile200DAVID ROBERTS, PHD

Scientific Operations Manager

David Roberts is the Scientific Operations Manager for the Tuberculosis Discovery Research Group and is the Biological Safety Officer for IDRI. His work includes management of the BioSafety Level 2 and 3 laboratories, including training personnel.

Originally from Kenbridge, VA, David obtained his BSc in Biology from Virginia Tech in Blacksburg, VA. He then went on to perform his graduate studies on the mechanisms of pathogenesis of Borrelia spp. causing Lyme disease in the Department of Microbiology and Immunology at the Medical College of Virginia under the supervision of Dr. Richard Marconi. David came to the Northwest and performed his postdoctoral studies under David Sherman at the University of Washington, where he learned the ins-and-outs of Mycobacterium tuberculosisbiology and pathogenesis.

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Bio-BMcNeil200MATTHEW MCNEIL, PHD

Postdoctoral Scientist

Matthew is a Postdoctoral Scientist in the TB Discovery Research group at IDRI. By isolating drug resistant bacteria, Matthew’s work focuses on the identification and characterization of drug targets and mechanisms of drug resistance.

Matthew received his BSc in Genetics and PhD in Microbiology from the University of Otago, New Zealand. His graduate work with Dr. Peter Fineran focused on microbial metabolism. Prior to Joining IDRI, Matthew worked at the Institut de Biologie Integrative de la Cellule, France with Dr. Frederic Boccard applying super resolution microscopy to study the temporal and spatial localization of proteins involved in bacterial chromosome organization.

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Njikan-Profile200SAMUEL NJIKAN, PHD

Postdoctoral Scientist

Samuel Njikan is a Postdoctoral Scientist at IDRI. His main work focuses on developing an artificial lymph node system for the assessment of responses to human vaccines. In addition, Samuel also investigates the direct effect of adjuvant treated macrophages on the growth inhibition of disease causing pathogens such as Mycobacterium tuberculosis, West Nile Virus, Leishmania and Influenza virus.

Samuel obtained a Bachelor of Medical Laboratory Sciences (BMLS) from the University of Buea in Cameroon. He then moved to Cape Town, South Africa where he obtained a Master of Science in medicine in the field of hematology and a PhD in clinical science and immunology all from the University of Cape Town. His PhD thesis with Prof. Willem Hanekom aimed at identifying correlates of risk of TB disease in infants with differential response to BCG vaccination.

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Shetye-Profile200GAURI SHETYE, PHD

Postdoctoral Scientist

Gauri Shetye is a Postdoctoral Scientist in the TB Discovery Research group at IDRI. Gauri's work focuses on identifying new drug targets against tuberculosis and understanding the mode of action against such targets.

Gauri received her BSc and MSc in Chemistry from University of Mumbai and her PhD in Chemistry from Syracuse University. In her PhD study under professor Yan-Yeung Luk, Gauri deployed small molecules for modulating the multicellular behaviors of bacteria like biofilm formation and swarming motility. She also investigated the mode of action for such small molecules in controlling bacterial behaviors.

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Zuniga-Profile200EDISON S. ZUNIGA, PHD

Postdoctoral Scientist

Edison S. Zuniga is a Postdoctoral Chemist in the Tuberculosis Drug Discovery Group. His work is focused on the elucidation of drug targets and modes of action, as well as the synthesis and discovery of novel biologically active compounds that work against Mycobacterium tuberculosis.

Edison has expertise in synthetic and medicinal chemistry. He received a BS in chemistry and a BA in English from the University of Washington and his PhD in organic chemistry at Stony Brook University. Under the supervision of Distinguished Professor Iwao Ojima, his graduate research focused on the design, synthesis and biological evaluation of novel taxoids and taxoid-based drug conjugates. While working in the Ojima lab, he also studied cancer stem cell biology with Dr. Galina Botchkina.

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Jill AshmanJill Ashman, MS

Director, Clinical Operations

Jill has worked in the field of international health and development, infectious diseases and clinical trials for over 40 years. After working as a bench scientist in clinical chemistry she joined the Voluntary Services Overseas and worked in Latin America as a professor of biology and biochemistry and on UNICEF field studies. Jill was the co-founder of Agrosalud, a non-profit health care program in rural Guatemala and collaborated with the University of Miami Field Epidemiology Survey Team on projects in the San Blas archipelago in Panamá, including cholera intervention, scabies and head lice studies. After working more than a decade in the field of HIV and AIDS, coordinating HIV vaccine trials at SCHARP, she joined IDRI in 2003 to set up and manage clinical vaccine trials.

Jill earned a BSc first class Honours degree in Zoology from the University of St. Andrews and a MS in Epidemiology from the University of Washington.

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Zachary SawagaZachary Sawaga, MS

Manager, Regulatory

Zack is IDRI’s Regulatory Manager, part of the team that enables moving IDRI’s vaccines from the lab into human clinical trials. He is responsible for regulatory submissions and all other interactions with regulatory authorities around the world. He provides support to clinical development and operations efforts, including writing and editing funding proposals, protocols, informed consent forms, and many other types of clinical trial documentation. He also oversees the design and execution of GLP toxicity studies, a critical final step before IDRI’s vaccines can be tested for safety and efficacy in humans.

Zack has an M.S. in Biomedical Regulatory Affairs from the University of Washington. His background is in biological science research, having completed an M.S. in Biology from the Rockefeller University and several years’ experience as a Research Scientist in academia. He graduated with a B.S. in Cell and Molecular Biology from the University of Washington, where he was a Howard Hughes Medical Institute Undergraduate Research Fellow.

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