Mia McLeod, COA

Clinical Research Coordinator at Georgia Retina, PC
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Contact Information
us****@****om
(386) 825-5501
Location
Atlanta, Georgia, United States, GE

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Credentials

  • Medidata Classic Rave EDC Essentials for Clinical Research Coordinators
    Medidata Solutions
    Sep, 2022
    - Oct, 2024
  • IATA Transportation of Dangerous Goods
    Mayo Clinic Laboratories
    Aug, 2022
    - Oct, 2024
  • Investigator Site Personnel ICH GCP Training Certificate
    TransCelerate BioPharma Inc.
    Aug, 2022
    - Oct, 2024
  • Certified Ophthalmic Assistant (COA)
    IJCAHPO
    Feb, 2014
    - Oct, 2024
  • Ophthalmic Scribe Certified (OSC)
    IJCAHPO
    Jan, 2016
    - Oct, 2024

Experience

    • United States
    • Medical Practices
    • 1 - 100 Employee
    • Clinical Research Coordinator
      • Feb 2023 - Present

      • Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified timeframe indicated in the study contract. • Coordinates monitor site visits and assists with preparation of site visit documentation. • Manages and maintains all regulatory information about the study including the protocol, investigator brochure, IRB documents, Investigator disclosures,CVs, training documentation, instructions on reporting requirements for the IRB/sponsor. • Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and/or IRB within required timeframe. • Ensures study staff is properly trained on study related information (i.e., protocol, ICF, manuals, etc.) with proper documentation of all trainings. • Conduct pre-study, initiation and close out visits with sponsor representatives. • Ensures compliance with all FDA and GCP guidelines. • Screening, recruiting and enrolling study participants while ensuring compliance with inclusion/exclusion criteria. • Work collaboratively with external sponsors, regulatory agencies, and contract research organizations. • Completes the informed consent process and administers questionnaires. • Coordinate study visits with subjects including scheduling appointments, securing study materials and conducting study related procedures. • Educates research participants and families on protocol, study intervention, study drug/device, etc.• Maintain compliance with all research StandardOperating Procedures (SOPs). • Adhere to Good Clinical Practice (GP) guidelines including regulatory and ethical standards. Show less

    • Clinical Research Assistant
      • Aug 2022 - Feb 2023

      • Screening, tracking and scheduling subjects. • Obtaining physician signatures.• Processing laboratory data and shipping biological samples. • Performing study procedures in a detailed and accurate manner.• Maintaining study files.• Maintaining correspondence and communication with subjects, sponsors, monitors and other site/study personnel.• Assisting study monitors with CRA corrections on regulatory forms or other documents. • Monitoring study specific supplies. • Anticipating the needs of coordinators and management by gathering records, reports, correspondence or other specific information. Show less

    • United States
    • Medical Practices
    • Technician Supervisor/Lead
      • May 2019 - Jul 2022

      • Create job postings, review resumes and assist in the hiring process • Technician training • Pre/Post operative surgical counseling • Review charting, coding and maintain accuracy in the EMR system • Manage patient/ technician schedule • Facilitate proper clinic function • Triage calls and handle concerns • Create job postings, review resumes and assist in the hiring process • Technician training • Pre/Post operative surgical counseling • Review charting, coding and maintain accuracy in the EMR system • Manage patient/ technician schedule • Facilitate proper clinic function • Triage calls and handle concerns

    • United States
    • Medical Practices
    • 200 - 300 Employee
    • Ophthalmic Technician
      • Mar 2017 - Dec 2018

      • Perform patient workups including visual acuity, refractions, pupil assessment, EOM's and applanation tonometry. • Prep for and assist with in office surgical procedures • Execute diagnostic testing such as visual fields, OCT, fundus photos, pachymetry and topography • Transmit prescriptions for medication and instruct patients on usage • Properly scribe physician findings during exams • Perform patient workups including visual acuity, refractions, pupil assessment, EOM's and applanation tonometry. • Prep for and assist with in office surgical procedures • Execute diagnostic testing such as visual fields, OCT, fundus photos, pachymetry and topography • Transmit prescriptions for medication and instruct patients on usage • Properly scribe physician findings during exams

Education

  • Clayton State University
    Bachelor's degree, Integrative Studies
    2016 - 2019
  • Durham Technical Community College
    Associate's degree, General Studies
    2010 - 2012

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