Meriza V.
Director Clinical Operations at Excision BioTherapeutics- Claim this Profile
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Topline Score
Bio
Experience
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Excision BioTherapeutics
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United States
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Biotechnology
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1 - 100 Employee
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Director Clinical Operations
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Jun 2021 - Nov 2023
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Bristol Myers Squibb
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United States
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Pharmaceutical Manufacturing
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700 & Above Employee
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Clinical Operations Consultant
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Nov 2020 - Jun 2021
Acquired MyoKardia in November 2020 Acquired MyoKardia in November 2020
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MyoKardia
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United States
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Biotechnology Research
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1 - 100 Employee
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Clinical Operations Consultant
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Sep 2018 - Nov 2020
US clinical operations lead for the pivotal Phase III and long-term extension studies in obstructive hypertrophic cardiomyopathy program. Camzyos (mavacamten) FDA approved, 2022. via Advanced Clinical US clinical operations lead for the pivotal Phase III and long-term extension studies in obstructive hypertrophic cardiomyopathy program. Camzyos (mavacamten) FDA approved, 2022. via Advanced Clinical
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Genentech
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United States
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Biotechnology Research
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700 & Above Employee
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Contract Global Studies Manager
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Apr 2015 - Apr 2018
Global manager for two late-stage natural history studies observing patients with age-related macular degeneration. Partnered with country affiliates in Argentina, Brazil, Colombia, Australia, Poland, France, Germany, and UK. via PRO Unlimited Global manager for two late-stage natural history studies observing patients with age-related macular degeneration. Partnered with country affiliates in Argentina, Brazil, Colombia, Australia, Poland, France, Germany, and UK. via PRO Unlimited
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Gilead Sciences
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United States
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Biotechnology Research
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700 & Above Employee
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Clinical Research Contractor
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Dec 2012 - Dec 2014
In-house operations support for two late phase global registry studies observing patients treated for hepatitis C. Sovaldi (sufosbuvir) FDA approved, 2013. via Aerotek Scientific In-house operations support for two late phase global registry studies observing patients treated for hepatitis C. Sovaldi (sufosbuvir) FDA approved, 2013. via Aerotek Scientific
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InterMune
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Biotechnology
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1 - 100 Employee
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Clinical Research Contractor
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Feb 2012 - Jul 2012
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FibroGen, Inc.
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United States
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Biotechnology Research
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300 - 400 Employee
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Senior CRA
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Jan 2011 - Aug 2011
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Novartis
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Switzerland
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Pharmaceutical Manufacturing
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700 & Above Employee
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Clinical Trial Manager
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Mar 2010 - Jan 2011
Clinical trial manager in the influenza vaccine program, including seasonal, pre-pandemic (H5N1) and pandemic (H1N1) influenza vaccine studies.
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Clinical Research Associate
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Oct 2005 - Feb 2010
Contributions acknowledged in "A dose-ranging study of MF59-adjuvanted and non adjuvanted A/H1N1 pandemic influenza vaccine in young to middle-aged and older adult populations to assess safety, immunogenicity, and antibody persistence one year after vaccination," Human Vaccines and Immunotherapeutics, 2014.
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PPD
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United States
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Research Services
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700 & Above Employee
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Clinical Research Associate
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Feb 2001 - Aug 2005
Study monitor conducting on-site visits for Phase III studies in pediatric vaccines and prostate cancer. Based in Cambridge UK from 2004 to 2005. Study monitor conducting on-site visits for Phase III studies in pediatric vaccines and prostate cancer. Based in Cambridge UK from 2004 to 2005.
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Education
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University of California, Berkeley
BA, Molecular and Cell Biology