Rachel Fuchs - Clinical Research Coordinator Resume Simple
A highly motivated, detail-oriented professional with over 15 years of experience in the healthcare industry. I am a self-starter, able to prioritize and prioritize multiple tasks.
  • management, communication, documentation, manager, patient, reporting, patient care
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Conner High School

    • Maintains accurate and timely communication with study sponsors, CRA/project Manager, and sponsor. Documentation of all study related activities.
    • Ensure that all study related activities and data management are in compliance with the protocol and the guidelines of the protocol and the overall conduct of the study.
    • Manage patient care activities, including but not limited to, vital signs, blood draws, and specimen processing.
    • Maintain accurate and complete records of study activities, case report forms, and serious adverse events. Participate in the development of protocol and reporting tools.
    • Assist in the preparation of study documents for submission to IRB. Review regulatory documents for completeness and accuracy. Responsible for ensuring that all study related forms are completed and filed.
    • Review and approve regulatory documents for submission to IRB and sponsor. Manage study related activities. Assist with the preparation of IRB submissions, renewals, amendments, serious adverse events, and serious adverse events.

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