Teodora Vaughn - Research Fellow Resume Simple
SUMMARY
I am a highly motivated, detail-oriented, and results-driven professional with over 15 years of experience in the pharmaceutical industry.
SKILLS
  • literature review, presentations, assessment, spss, pharmacy, research, geriatrics, analysis, database, statistical analysis, writing, nursing, clinical research, clinical
  • liaison, monitoring, documentation, patient, shipping, patient care, research, medical devices, manufacturing, computer, database, compliance, dialysis, coordinator, medical, clinical
WORK EXPERIENCES
  • 2017-12-252017-12-25

    Research Fellow

    Vector Marketing

    • Conducted research and analysis of HIV/AIDS patients in the nursing homes and the biomedical department. Collaborated with the National cancer Institute to develop a comprehensive assessment of the HIV-infected patient.
    • Assisted in the development of the research project and the implementation of the clinical research database for the biomedical and quantitative data.
    • Participated in the development of a research project for the use of the C-arm in the biomedical. Worked with the R&D team to develop a new method for the evaluation of the human female.
    • Performed statistical analysis on data for publication in the journal of public health. Participated in the development of a new SAS program.
    • Conducted literature searches, presentations, and journal articles for the R&D Committee. Participated in the development of new research protocols.
    • Presented at the University of Iowa school of health Sciences research conference.-presented at the American Society of public health.
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Biola University

    • Managerial responsibilities included: Monitoring of study subjects, documentation of adverse events, and ensuring compliance with protocol, clinical and regulatory guidelines.
    • Assisted in the management of clinical trials, including patient safety monitoring, regulatory document review, and study start-up activities.
    • Acted as a liaison between the clinical research Associate and the sponsor and the production team. Provided technical support to the investigational site and medical staff.
    • Assist in the collection of data from the study sites. Notifies supervisor of any adverse events. Notify investigators of serious adverse events.
    • Provided support to the investigational sites and the sponsor as needed. Performed data entry and QA/QC audits of the clinical trials.
    • Ensured that all managerial documentation was completed and maintained in a timely manner. Performed QA/QC checks. Assisted in the preparation of study materials.

  

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