Joe Palca
Joe Palca is a science correspondent for NPR. Since joining NPR in 1992, Palca has covered a range of science topics — everything from biomedical research to astronomy. He is currently focused on the eponymous series, "Joe's Big Idea." Stories in the series explore the minds and motivations of scientists and inventors. Palca is also the founder of NPR Scicommers – A science communication collective.
Palca began his journalism career in television in 1982, working as a health producer for the CBS affiliate in Washington, DC. In 1986, he left television for a seven-year stint as a print journalist, first as the Washington news editor for Nature, and then as a senior correspondent for Science Magazine.
In October 2009, Palca took a six-month leave from NPR to become science writer in residence at The Huntington Library, Art Collections, and Botanical Gardens.
Palca has won numerous awards, including the National Academies Communications Award, the Science-in-Society Award of the National Association of Science Writers, the American Chemical Society's James T. Grady-James H. Stack Award for Interpreting Chemistry for the Public, the American Association for the Advancement of Science Journalism Prize, and the Victor Cohn Prize for Excellence in Medical Writing. In 2019, Palca was elected to the American Academy of Arts and Sciences for outstanding achievement in journalism.
With Flora Lichtman, Palca is the co-author of Annoying: The Science of What Bugs Us (Wiley, 2011).
He comes to journalism from a science background, having received a Ph.D. in psychology from the University of California at Santa Cruz, where he worked on human sleep physiology.
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The Food and Drug Administration has made public drugmaker Moderna's application for emergency authorization of its COVID-19 vaccine. NPR explores what researchers think of the application.
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The FDA released detailed analysis of the vaccine ahead of a Thursday meeting of a group of independent experts that will advise the agency on whether to authorize the vaccine for emergency use.
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Americans are waiting for the first doses of Pfizer's coronavirus vaccine, expected to be distributed very soon. Moderna also has a vaccine waiting for federal review.
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An advisory committee of independent experts met on Thursday to consider an emergency use authorization for Pfizer's COVID-19 vaccine. NPR discusses the committee's deliberations and recommendations.
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The Food and Drug Administration released its analysis of the Pfizer coronavirus vaccine. An independent committee will meet with the agency Thursday to discuss emergency use of the vaccine.
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The Food and Drug Administration has released detailed information about the Pfizer/BioNTech Covid-19 vaccine. The material will be evaluated later this week by an independent committee of experts.
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Researchers found that a class of antibodies in a monkey's blood provides protection from COVID-19. If that hold true for humans, a blood test may predict whether a vaccine candidate is working.
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The White House coronavirus task force briefed reporters on Thursday for the first time in months as the Centers for Disease Control and Prevention warned Americans to avoid travel.
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The vaccine was found to be 95% effective in an updated study analysis. Safety data required by the Food and Drug Administration showed no serious concerns, the company said.
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The vaccine is nearly 95% effective in preventing illness, according to an interim analysis of a clinical test involving 30,000 people.