Meriza V.

Director Clinical Operations at Excision BioTherapeutics
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Contact Information
us****@****om
(386) 825-5501
Location
San Diego, California, United States, US

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Experience

    • United States
    • Biotechnology
    • 1 - 100 Employee
    • Director Clinical Operations
      • Jun 2021 - Nov 2023

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Clinical Operations Consultant
      • Nov 2020 - Jun 2021

      Acquired MyoKardia in November 2020 Acquired MyoKardia in November 2020

    • United States
    • Biotechnology Research
    • 1 - 100 Employee
    • Clinical Operations Consultant
      • 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

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Contract Global Studies Manager
      • 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

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Clinical Research Contractor
      • 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

    • Biotechnology
    • 1 - 100 Employee
    • Clinical Research Contractor
      • Feb 2012 - Jul 2012

    • United States
    • Biotechnology Research
    • 300 - 400 Employee
    • Senior CRA
      • Jan 2011 - Aug 2011

    • Switzerland
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Clinical Trial Manager
      • Mar 2010 - Jan 2011

      Clinical trial manager in the influenza vaccine program, including seasonal, pre-pandemic (H5N1) and pandemic (H1N1) influenza vaccine studies.

    • Clinical Research Associate
      • 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.

    • United States
    • Research Services
    • 700 & Above Employee
    • Clinical Research Associate
      • 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.

Education

  • University of California, Berkeley
    BA, Molecular and Cell Biology

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