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Atea Pharmaceuticals Expands Senior Management Team with Key Additions in Regulatory Affairs and Investor Relations and Corporate Communications

Senior executives bring proven industry experience to leadership roles in regulatory affairs and communications BOSTON, Jan. 19, 2021 (GLOBE NEWSWIRE) -- Atea

articleAtea Pharmaceuticals, Inc.January 19, 20213/company/atea-pharmaceuticals-inc/news/atea-pharmaceuticals-expands-senior-management-team-with-key-additions-in-regulatory-affairs-and-investor-relations-and-corporate-communications
Atea Pharmaceuticals Expands Senior Management Team with Key Additions in Regulatory Affairs and Investor Relations and Corporate Communications

About this update from Atea Pharmaceuticals, Inc.

[{"type":"text","content":"Senior executives bring proven industry experience to leadership roles in regulatory affairs and communications BOSTON, Jan. 19, 2021 (GLOBE NEWSWIRE) -- Atea Pharmaceuticals, Inc. (Nasdaq: AVIR) (“Atea”), a clinical-stage biopharmaceutical company, today announced that it has expanded its senior management team with the appointments of Jayanthi Wolf, Ph.D., Senior Vice President of Regulatory Affairs and Jonae Barnes, Senior Vice President of Investor Relations and Corporate Communications. “We are very pleased to welcome Jayanthi and Jonae to Atea,” said Jean-Pierre Sommadossi, Ph.D., Founder and Chief Executive Officer of Atea Pharmaceuticals. “They bring with them extensive and highly valuable industry experience, which will expand Atea’s capability as we continue to advance our corporate initiatives and our product candidates, including moving forward with the Phase 3 program for AT-527 for COVID-19 and AT-752 as a potential therapeutic for Dengue fever.” Dr. Wolf has had an extensive career in research and development at Merck over a 19-year period. During her tenure at Merck, she served in a series of roles ranging from scientific to safety assessment and regulatory, with increasing responsibility in global regulatory affairs and clinical safety. Dr. Wolf has broad experience in regulatory affairs, including clinical, nonclinical and manufacturing and has managed programs from preclinical development through regulatory approval. She served as the global regulatory team leader for several products, including ERVEBO®, the first Ebola vaccine approved by the U.S. Food and Drug Administration, the European Medicines Agency and prequalified by the World Health Organization. Dr. Wolf earned a Ph.D. and master’s degree in molecular biology and immunology from Princeton University and a B.S. in biochemistry from Susquehanna University. Ms. Barnes has more than 20 years of experience in the pharmaceutical and biotechnology industry. Her experience in strategic investor relations and corporate communications spans the full life cycle of drug development and commercialization. She began her career at Sepracor (now Sunovion Pharmaceuticals; acquired by Dainippon Sumitomo Pharma Co.), where she held a series of progressively responsible management and executive roles over a 14-year period and served most recently as Senior Vice Presid...

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