Teodora Vaughn - Research Fellow Resume Simple
I am a highly motivated, detail-oriented, and results-driven professional with over 15 years of experience in the pharmaceutical industry.
  • 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
  • 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.


Your resume is an essential part of the strategies through which you can make a job opening your own. However, creation of the perfect resume with the right information can be seriously time-consuming since you’d have to make sure that the hiring faculties are attracted by it in the first few seconds of viewing. This can involve focusing on the placement of the fields, the design of the overall resume, and of the length of the presentation of information in it.