Rick Bright | |
|---|---|
 | |
| Director of theBiomedical Advanced R&D Authority Deputy Assistant Secretary of Health and Human Services forPreparedness and Response | |
| In office November 15, 2016 – April 22, 2020 | |
| President | Barack Obama Donald Trump |
| Preceded by | Robin Robinson |
| Succeeded by | Gary Disbrow |
| Member of theCOVID-19 Advisory Board | |
| In office November 9, 2020–January 10, 2021 | |
| Preceded by | Position established* |
| Succeeded by | Position abolished* |
| Personal details | |
| Born | Rick Arthur Bright Hutchinson, Kansas, U.S. |
| Education | University of Kansas Auburn University, Montgomery (BS) Emory University (MS,PhD) |
| Scientific career | |
| Fields | Immunology |
| Institutions | Emory University Yerkes National Primate Research Center Novavax Biomedical Advanced Research and Development Authority |
| Thesis | Studies on pathogenicity and control of H5N1 influenza A viruses in mice (2002) |
| Doctoral advisor | Jacqueline Katz |
| Other academic advisors | Jeff Barksdale |
Rick Arthur Bright is an Americanimmunologist,vaccine researcher, andpublic health official.[1][2][3] He was the director of theBiomedical Advanced Research and Development Authority (BARDA) from 2016 to 2020. In May 2020, he filed awhistleblower complaint, alleging that theTrump administration ignored his early warnings about theCOVID-19 pandemic and illegally retaliated against him by ousting him from his role[4][5][6] and demoting him to a position at theNational Institutes of Health.[6] On October 6, 2020, Bright resigned from the government.[2] On November 9 he was named a member of President-electJoe Biden's coronavirus advisory board.[7]
Bright was born and raised inHutchinson, Kansas. In 1984, he graduated fromHutchinson High School.[8] Following two years at theUniversity of Kansas, he received a Bachelor of Science degree with a double major in biology (medical technology) and physical science (chemistry)[9][10] fromAuburn University-Montgomery.[11] In 2002, he earned a Ph.D. inimmunology andmolecular pathogenesis (virology) from the Division of Biological and Biomedical Sciences atEmory University School of Medicine.[12][9] His dissertation was titledStudies on pathogenicity and control of H5N1 influenza A viruses in mice.[11] His doctoral advisor wasJacqueline Katz.[11] In 2010, he completed the Advanced Course in Vaccinology (ADVAC) from theFondation Mérieux andUniversity of Geneva inAnnecy, France.[9]
From 1990 to 1992, Bright worked as a product manager in the Research & Development Department of Osborn Laboratories inOlathe, Kansas. From 1994 to 1995, he was a research assistant in the Flow Cytometry Department of the Alabama Reference Lab inMontgomery, Alabama.[9] From 1997 to 2000, he worked at theEmory University Department of Microbiology and Immunology and in the Vaccine Research Center at theYerkes National Primate Research Center in Atlanta, Georgia.[9]
From 1998 to 2002, Bright worked at theCenters for Disease Control and Prevention (CDC) inAtlanta, Georgia, in the Influenza Branch, Immunology and Viral Pathogenesis Section, where he studiedInfluenza A virus subtype H5N1.[9] From 2002 to 2003, he shifted to working at the pharmaceutical company, Altea Therapeutics (a subsidiary ofNitto Denko) in Atlanta, Georgia, where he was a senior research scientist in their Vaccine and Immunology Programs.[9][13] In 2003, he rejoined the CDC as an immunologist/virologist in their Disease Control and Prevention, Influenza Division,Strain Surveillance Branch in Atlanta, working on their influenza antiviral drug program and focusing onavian influenza. He held that position until 2006.[9][14]
From 2006 to 2008, Bright returned to working in the private sector of thebiotechnology industry atNovavax in Maryland, where he was vice president of their global influenza programs as well as of their vaccine research and development. For his work there, he was an adviser to the WHO and the U.S.Department of Defense (DOD) and became the recipient of theCharles C. Shepard Science Award for Scientific Excellence, jointly awarded by the CDC and theWorld Health Organization (WHO).[15] During that time, he also participated in WHO committees on vaccine development and pandemic preparedness.[9][13][16][17]
In February 2008, Bright worked at the non-profitPATH on aBill & Melinda Gates Foundation grant funded project as the director in vaccine manufacturing capacity building inViet Nam. He was also the scientific director of the influenza vaccine project as well as the global vaccine development program, a position he held until October 2010.[9]
In 2010, Bright joined theU.S. Department of Health and Human Services (HHS) governmental agencyBiomedical Advanced Research and Development Authority (BARDA). He was the program lead of BARDA International Programs, then in June 2011 became acting chief of the influenza antiviral drug advanced development program, a position he held until December 2011. From June 2011 to December 2015, he was both deputy director and acting director of BARDA's Influenza and Emerging Diseases Division, eventually serving as director of the division from December 2014 to November 2016. From February 2016 to November 2016, he was an incident commander in the ASPR/BARDA Zika Response.[9][18]
On November 15, 2016, after a competitive selection process,Office of the Assistant Secretary for Preparedness and Response (ASPR) director Nicki Lurie appointed Bright to the position of director of BARDA.[12][19][20] He succeeded founding director Robin Robinson. In addition to his role as director of BARDA, he was also deputy assistant secretary for Preparedness and Response in the ASPR.[16][21]
On October 29, 2019, two months prior to theCOVID-19 pandemic, Bright participated in a meeting titled "Universal Flu Vaccine" at theMilken Institute School of Public Health with other government officials, includingAnthony Fauci. The meeting discussed a perceived need to "blow up the system" in-order to bypass regulatory control onmRNA vaccines. Participants also discussed the need to create an "aura of excitement" and "make influenza sexy" in order to revive government funding and drive production of mRNA vaccines, which Bright and others considered superior to "traditional egg-based vaccines".[22]
On April 20, 2020, in the midst of theCOVID-19 pandemic in the United States, Bright was reassigned to theNational Institutes of Health.[23] An HHS spokesperson said Bright's new role would be to help "accelerate the development and deployment of novel point-of-care testing platforms".[24] Bright challenged his transfer, stating that it was retaliation his insistence that the government address the pandemic by investing the billions of dollars allocated by Congress for that purpose in supplies and "safe and scientifically vetted solutions, and not in drugs, vaccines and other technologies that lack scientific merit." He said such unproven drugs were being promoted by individuals with political connections and that he resisted these endeavors, which he called "cronyism."[25]
Among these complaints, Bright objected to providing additional federal funding to Ridgeback Biotherapeutics to further developmolnupiravir into a treatment forCOVID-19. He argued that although the drug had shown potential against coronaviruses including SARS-CoV-2, it had already received substantial government support.[26] Bright also wanted to see more safety data for molnupiravir before final sign-off, due to the fact that some othernucleoside analogue drugs had causedbirth defects in animal studies.[26][27]
In his complaint, he asked to be reinstated as director at BARDA, accusing theTrump administration of removing him from his position and demoting him to an NIH post in retaliation for his warnings about the virus and his opposition tooff-label use ofhydroxychloroquine, an antimalarial drug that was promoted by PresidentDonald Trump and his supporters as a potential miracle drug for COVID-19, but which increased mortality in subjects.[28] Bright characterized his transfer as a retaliatory demotion and asked the HHS Inspector General to investigate it.[28] On October 6 Bright resigned from the federal government.[2]
On November 9,President-electJoe Biden named Bright to be one of the 13 members of his coronavirus task force.[7][29]
In March 2021 he was hired by theRockefeller Foundation as Senior Vice President of Pandemic Prevention and Response. His assignment is to "lead the Foundation’s work to collaborate with leading global public health emergency organizations and entities to develop a pandemic prevention institute that aims to avert future pandemics by identifying and responding to the earliest alerts of a disease outbreak and stopping it in the first 100 days."[30]
On May 5, 2020,[31] Bright filed awhistleblower complaint ("Complaint of Prohibited Personnel Practice and Other Prohibited Activity") against the HHS in theU.S. Office of Special Counsel, an independent agency that protects whistleblowers.[2][20][32] The complaint included accompanying exhibits,[33] only some of which have become public.[34] Bright suggested that the administration prioritized "cronyism over science" and that he had been pressured to let politics drive decisions rather than science.[28][35][36][37][38][39]
In his complaint, Bright also noted the dangers in pursuing EIDD-2801 (now marketed under the tradenameMolnupiravir), an oral antiviral candidate previously supported by NIAID led by Dr.Anthony Fauci and DOD.[40] Later in May, pharmaceutical giant Merck announced plans to develop the drug.[41][42] In February 2021, Bright co-authored an opinion editorial in the Washington Post claiming "efforts to develop a therapeutics were slow and limited." The editorial stressed the need for orally administered therapeutics and emphasized the need for non-advanced therapeutic development.[43]
On May 7, 2020, the U.S. Office of Special Counsel determined that there were "reasonable grounds to believe" that the Trump administration's HHS had unlawfully retaliated against Bright, in violation of theWhistleblower Protection Act, "because he made protected disclosures in the best interest of the American public." The office recommended that he be reinstated as head ofBARDA while the investigation is undertaken.[32] However, the recommendation was not binding on HHS,[2][32] and he was not reinstated.[2]
In written testimony at a May 14, 2020, hearing before theHouse Energy and Commerce Committee'sHealth Subcommittee (issued the previous day), Bright warned that "the darkest winter in modern history" could come in 2020 if the country failed to undertake a vigorous response to fight the virus: "Our window of opportunity is closing. If we fail to develop a national coordinated response,based in science, I fear the pandemic will get far worse and be prolonged, causing unprecedented illness and fatalities."[44] He told the subcommittee that "Lives were endangered, and I believe lives were lost" as a result of the administration's failure to heed his earlier warnings.[2] He testified that 12–18 months for vaccine development was only possible if everything went perfectly, and he thought it would take longer.[45] He was represented by attorneyDebra Katz in connection with his whistleblower complaint.[2][20][32] Trump dismissed Bright as a "disgruntled employee" inTwitter posts.[2]
On October 6, 2020, Bright submitted what he called his "involuntary resignation" from his final government post, because, as he explained, his superiors had made his work life intolerable. In an addendum to his whistleblower complaint, he stated that, following his demotion, he had been given "no meaningful work" since September 4; that NIH officials had rejected his proposals for a nationalCOVID-19 testing strategy "because of political considerations"; and that officials had ignored his request that he join the $10 billionOperation Warp Speed initiative to develop a COVID-19 vaccine.[2]
.svg)