Glenda Welty - Clinical Research Coordinator Resume Simple
SUMMARY
A highly motivated, detail-oriented professional with over 15 years of experience in the clinical research industry. I am a self-starter, able to prioritize and prioritize effectively and efficiently.
SKILLS
  • management, ultrasound, workflow, data collection, design, collection, responsible, research, quality, supervision, project management, edc, computer, compliance, technology, medical records, fda, patient, vital signs, medical, clinical
  • powerpoint, clinical operations, microsoft, sops, operations, microsoft word, excel, gcp, word, administrative, clinical, ich
WORK EXPERIENCES
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Cummins

    • Provide assistance to the Principal investigator in the design, implementation and evaluation of research protocols, including but not limited to, patient recruitment, consent, consent, and medical history, vital signs, ECG, blood
    • Perform clinical research activities including but not limited to: Protocol design, study specific procedures, study initiation, interim monitoring, and compliance with the protocol.
    • Responsible for the implementation of research protocols, quality of data, and study design for the clinical trial. Conduct and review of the protocol, including the development of the workflow and the integration of the data.
    • Assist in the development and implementation of clinical research protocols. Conduct study initiation, interim, and close out visits.
    • Work with the Principal investigator and sub-investigators in the implementation of the research protocol and the medical record review process.
    • Assist in the development and implementation of the study management plan and the production of the study protocol. In addition to the following: I have been trained to perform the duties of the clinical trial.
  • 2017-12-252017-12-25

    Clinical Trial Assistant

    University of Washington

    • Maintain and update study databases, including but not limited to, regulatory binders, study specific files, and other documents.
    • Ensure that all clinical research activities are conducted in compliance with ICH/GCP guidelines. Assist in the preparation of study reports.
    • Assist with the preparation of study related documents, including study management and other documents. Prepare and submit all required reports to the site.
    • Assists with the development and maintenance of research operations and databases. Performs other related duties as assigned. Performs other related tasks as assigned.
    • Perform administrative tasks such as Word processing, spreadsheet, and Excel. Maintain databases and spreadsheets. Track and report all data and reports.
    • Review and edit study documents in the clinical trial Master file (TMF). Ensure that all the documents are complete and filed in the appropriate files.

 Neeyamo 

 Susquehanna Bancshares, Inc.