Chidera Obi

APEX Clinical Research Associate at Parexel
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Contact Information
us****@****om
(386) 825-5501

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Experience

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • APEX Clinical Research Associate
      • Feb 2023 - Present

  • SMS Clinical Research
    • Mesquite, Texas, United States
    • Clinical Research Coordinator
      • Jul 2022 - Feb 2023

      Support, facilitate, and coordinate daily clinical trial activities as instructed in SOPs. Collecting data, and informing participants about study objectives. Support, facilitate, and coordinate daily clinical trial activities as instructed in SOPs. Collecting data, and informing participants about study objectives.

    • United States
    • Hospitals and Health Care
    • 1 - 100 Employee
    • Clinical Research Coordinator
      • Mar 2022 - Jul 2022

      Utilized skills taught in extensive Clinical Research Coordinating Program. Recruiting, consenting, and inputting data of patients qualified for the study being conducted at the research clinic. Utilized skills taught in extensive Clinical Research Coordinating Program. Recruiting, consenting, and inputting data of patients qualified for the study being conducted at the research clinic.

    • United States
    • Hospitals and Health Care
    • 1 - 100 Employee
    • Lead Mental Health Technician
      • Oct 2021 - Jul 2022

      Chart patient observations, following prescribed procedures and standards. Provide care to patients in a manner that promotes safety, comfort, and a therapeutic environment. Assist patients with activities of daily living. Assisted in skin checks, collecting vitals, and preparing patients for examination by performing preliminary physical tests; taking blood pressure, weight, and temperature. Chart patient observations, following prescribed procedures and standards. Provide care to patients in a manner that promotes safety, comfort, and a therapeutic environment. Assist patients with activities of daily living. Assisted in skin checks, collecting vitals, and preparing patients for examination by performing preliminary physical tests; taking blood pressure, weight, and temperature.

    • Clinical Research Coordinator Program
      • May 2022 - Jun 2022

      Regulatory Understanding: Comprehensive knowledge of FDA, GCP and HIPAA as applied to clinical research Clinical Research: Understanding of clinical research processes, along with knowledge of all functional areas of clinical trials including current ICH GCP guidelines. Safety: Knowledge of safety hazards and procedures that establish a safe work environment Computer Literacy: Proficiency in Microsoft Office (Word, Excel, Powerpoint, etc…), Adobe Suite Data Collection: Skilled in computer and data collection software Clinical: Phlebotomy and other technical skills as required per protocol

Education

  • University of North Texas
    Bachelor of Science - BS, Public Health

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