Victoria Washington

Experience

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  Ultra Body Fitness

  Jan 2019 - Jan 2019

  Assistant Fitness Director

  • Provided health screens for potential clients • Documented conversations between staff and clients• Organized and updated client information binders

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  ATI Physical Therapy

  Jan 2019 - Jan 2020

  Clinical Assistant

  • Assisted clinicians with executing patient exercise flowsheets• Updated patient charts using ATI EMR • Provided clinical administrative support to the clinicians

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  Eurofins | CRL, Inc.

  Jan 2020 - Jan 2021

  • Drafted study protocols, Informed Consent Forms (ICFs), and other trial-supporting documents for Institutional Review Board (IRB) submissions of GCP-compliant studies.• Followed all protocol and Standard Operating Procedure (SOPs), reported any deviations promptly to the Principal Investigator.• Transfered all raw data, documentation, protocols, and final reports to the Archivist at the close of the study. • Obtained background health information from prospective study subjects to evaluate their eligibility to participate in Eurofins CRL, Inc. clinical trials.• Coordinated with Principal Investigator to ensure adequate subject recruitment has been met for each study.• Obtained HIPAA Authorization from prospective study subjects and interview prospective study subjects.

  • Clinical Research Coordinator- Clinical Services

    Mar 2021 - Jan 2021

  • Clinical Research Coordinator- Recruiter

    Jan 2020 - Mar 2021
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  Syneos Health

  Jan 2021 - Jan 2024

  • Set-up, maintained and/or closed out project files and study information ((e.g., regulatory documents, Trial Master File (TMF), enrollment, Adverse Events (AEs)/Serious Adverse Events (SAEs), site supplies, Institutional Review Board re-approvals, data queries) on a variety of databases and systems.• Attended, participated, prepared and distributed meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator meetings). Followed up with team members on action items to closure.• Maintained timely and effective communication among team members and site staff. Kept Project Leadership and Clinical Research Associates (CRAs) fully appraised of sites and study status. May contact site staff as needed for critical information.• Provided administrative support to Project Leads and functional leads.• Ensured all study documents were archived based on the appropriate guidelines and policy. • Provided support for quality assurance activities, including preparation for audits and internal review, prepare documentation and follow through to resolution on actionable issues. Meno dettagli

  • CRA II

    Jan 2023 - Jan 2024

  • CRA I

    Jan 2022 - Jan 2023

  • Project Specialist

    Jan 2021 - Jan 2022
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  Parexel

  Jan 2024 - now

  CRA II