Andrea Levin, CCRC

Clinical Site Operations Manager at Meridian Clinical Research
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Contact Information
us****@****om
(386) 825-5501
Location
Hilton Head Island, South Carolina Area

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Credentials

  • Registered Technologist - Computed Tomography (RTBD)
    Nuclear Medicine Technology Certification Board (NMTCB)
    Jun, 2019
    - Oct, 2024
  • Certified Nuclear Medicine Technologist (CNMT)
    Nuclear Medicine Technology Certification Board (NMTCB)
    May, 2018
    - Oct, 2024
  • BLS Provider
    American Heart Association
    Jan, 2017
    - Oct, 2024
  • Certified Clinical Research Coordinator (CCRC)
    ACRP - Association of Clinical Research Professionals
    Oct, 2022
    - Oct, 2024
  • Pharmacy Technician
    Division of Professional Registration
    May, 2017
    - Oct, 2024

Experience

  • Meridian Clinical Research
    • United States
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Clinical Site Operations Manager
      • 2022 - Present

      Serve on leadership team with active involvement in developing processes and training to help new hires learn the essential functions of their role and actively contribute towards reaching the studies’ endpoints and objectives. Manage $500K site budgets to ensure positive-growth and cost-effective decisions.

    • Lead Clinical Research Coordinator
      • 2022 - 2022

      Maintained role as a Clinical Research Coordinator on multiple studies under 5 Principal Investigators while also taking on additional managerial tasks.

    • Clinical Research Coordinator
      • 2021 - 2022

      Served as primary Clinical Research Coordinator for 10 concurrent studies. Ensured attainment of deadlines and effectiveness of staff training. Travelled between sites to recruit eligible patients for various studies, ensuring high study enrollment. Executed data entry and performed various clinical tasks in accordance with the ICH E6 guidelines.

  • Coastal Neurology
    • United States
    • Hospitals and Health Care
    • 1 - 100 Employee
    • Clinical Research Coordinator
      • 2020 - 2021

      Performed all aspects of the research process from study start-up to study closing. Initiated regulatory document creation and submission as required for study conduct. Communicated with the Principal Investigator and sponsor to ensure the study protocol, accurately entered data into vendor systems and addressed data queries in a timely manner. Performed all aspects of the research process from study start-up to study closing. Initiated regulatory document creation and submission as required for study conduct. Communicated with the Principal Investigator and sponsor to ensure the study protocol, accurately entered data into vendor systems and addressed data queries in a timely manner.

  • Invivo Molecular Imaging
    • United States
    • Hospitals and Health Care
    • 1 - 100 Employee
    • PET/CT Technologist
      • 2018 - 2019

      Responsible for performing daily quality control procedures for cameras and hot labs and troubleshooting camera malfunctions. Fostered trust with radiologists and nuclear medicine departments at multiple hospitals and ensured that patient care adhered to the specific protocols of each site. Responsible for performing daily quality control procedures for cameras and hot labs and troubleshooting camera malfunctions. Fostered trust with radiologists and nuclear medicine departments at multiple hospitals and ensured that patient care adhered to the specific protocols of each site.

Education

  • University of Missouri-Columbia
    Nuclear Medical Technology/Technologist
    2014 - 2018

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