About AMWA – Board of Directors & Staff

Elizabeth (Beth) Garner, MD, MPH

Treasurer, 2020 – 2021

Dr. Elizabeth Garner has over a decade of pharmaceutical development experience, holding roles of increasing strategic responsibility in large and small companies, including ObsEva SA, Merck, Abbott (AbbVie), Myriad Genetics, and Agile Therapeutics, developing deep expertise in clinical trial design and execution. She joined ObsEva, a women’s health pharmaceutical company based in Geneva, Switzerland, in July 2019.  As Chief Medical Officer, she oversees all medical aspects of the company’s clinical development programs. Prior to ObsEva, she was Chief Medical Officer at Agile Therapeutics, where she led the company’s clinical development, regulatory, and medical affairs strategies. Dr. Garner designed and led the conduct of the Phase 3 SECURE trial, which supported FDA approval of the Twirla® contraceptive patch in February, 2020.

Prior to her tenure at Agile, Dr. Garner was Vice President, Medical Affairs, Women’s Health/Preventive Care at Myriad Genetic, where she managed the women’s health research, publication, and Key Opinion Leader (KOL) development programs, provided medical and scientific input on Myriad’s marketing and new product strategies, served as its media spokesperson, and directed an experienced team of Field Medical Specialists. Prior to that, she was Senior Director at Abbott Laboratories, where she oversaw all clinical aspects of the global Phase 3 endometriosis development program for Orilissa®.  From 2007 to 2011, Dr. Garner was Associate Director and then Director, Clinical Research at Merck Research Laboratories. As a leader on the human papillomavirus (HPV) vaccine program she was instrumental in achieving successful outcomes on important regulatory submissions. Dr. Garner also served as chair of the Gardasil®9 HPV vaccine program Product Development Team, leading scientific, regulatory, global access and medical affairs strategies. Dr. Garner was the core presenter for the 2010 FDA Gardasil® Advisory Committee Meeting for which she developed and delivered the company’s presentation that supported FDA’s approval of a gender-neutral indication for the prevention of HPV-related anal cancer. She also had substantial involvement in KOL development, provided medical input on commercialization strategy, and participated in due diligence activities on women’s health products.

Dr. Garner is a member of the Board of Directors of Kezar Life Sciences, a San Francisco based pharmaceutical company developing novel small molecule therapeutics for autoimmune diseases and cancer.  She is also on the Boards of the Drug Information Association (DIA), CorStone (an international non-profit focused on resilience in girls), and the Executive Women of New Jersey.  She was a 2019 awardee of the PharmaVoice 100 most inspiring individuals in the life-sciences industry.

Dr. Garner received joint M.D. and M.P.H degrees from Harvard Medical School and the Harvard School of Public Health. She was trained in obstetrics and gynecology at Brigham and Women’s/Massachusetts General Hospitals and completed a fellowship in gynecologic oncology at Brigham and Women’s and Dana Farber Cancer Institute. Prior to entering the pharmaceutical industry, Dr. Garner spent several years in academic clinical practice, basic science research in ovarian cancer, and teaching and mentorship at Harvard Medical School. She is an author on numerous peer-reviewed scientific publications.

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