Lucy Okie - Researcher Resume Simple
I am a highly motivated, detail-oriented, and results-driven professional with over 10 years of experience in the pharmaceutical industry.
  • manager, patient, design, communication, nutrition
  • analysis, communication, iv, patient, dialysis, reporting, responsible, research
  • 2017-12-252017-12-25


    Desoto County Schools

    • Developed a patient-centered care plan for the design of communication between the study and the principle Investigator. Developed a novel protocol for the prevention of breast cancer.
    • Participated in the development of nutrition and health care Manager and other study protocols. Assisted in the development of the informed consent process.
    • Developed and maintained relationships with key stakeholders to ensure the success of the project. Collaborated with the Principal investigator and the public to develop and implement the recruitment strategy.
    • Conducted literature reviews on the effects of the food and beverage consumption. Presented findings at the National conference. Participated in the development of a new website.
    • Conducted study visits to determine eligibility for study participants. Assisted with the preparation of IRB submissions. Ensured that all serious adverse events were reported.
    • Provided support to the community and the public to develop a healthy lifestyle and wellness program. This included the prevention of obesity and weight loss.
  • 2017-12-252017-12-25

    Research Coordinator

    YMCA of Greater Houston

    • In-depth knowledge of the principles of the therapeutic communication and patient rights. Developed and implemented a comprehensive assessment of the study.
    • Served as a primary contact for research study sponsors and responsible for data analysis and reporting. Developed and implemented corrective action plans for the department.
    • Conducted IV insertion and blood draws for patients with sickle cell disease and Alzheimer’s disease. Assisted in the development of a new study protocol.
    • Provide assistance to the dialysis department in the preparation of manuscripts. Assists in the development of grant proposals. Monitors and tracks grant funding.
    • Assisted in the development of study protocols, informed consent forms, and case report forms for clinical trials. Conducted data collection and analysis for study subjects.
    • Conducted literature searches and presented findings to the Principal Investigator. Wrote and edited grant proposals. Prepared and submitted grants for funding.