Chrysta Vo

Quality Control Manager II at Clinical Research IO

Chrysta Vo has worked in various roles in the clinical research field since 2009. Chrysta began their career as a Customer Sales Representative at Ameritran USA Inc. In 2016, they joined ProScience Research Group as a Clinical Research Coordinator, where they were responsible for ensuring all study procedures were conducted accurately in accordance with FDA, ICH, and GCP guidelines. In 2018, Chrysta joined Collaborative Neuroscience Network, LLC. as a Clinical Quality Assurance Coordinator. In this role, they created and reviewed source documents per protocols, and reviewed clinical data, investigator site files, informed consents, case report forms, monitoring letters, medical records, pK logs, lab reports, and study drug accountability. In 2021, Chrysta began working as a Study Design Reviewer (QC) at Clinical Research IO.

Chrysta Vo obtained a Bachelor of Science in Biochemistry from California State University, Long Beach between 2013 and 2015. Chrysta also holds certifications in CITI Training (obtained in March 2016), Certified Phlebotomy Technician from National HealthCare Associates (obtained in March 2016), CPR from American Red Cross (obtained in January 2016), and Laser Medication Assistant from Mac Beam Inc (obtained in March 2015).

Links

Timeline

  • Quality Control Manager II

    June 1, 2023 - present

  • Study Design Reviewer (QC)

    September, 2021

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