Estella Welle - Clinical Research Coordinator Resume Simple
A clinical research coordinator with a strong background in the pharmaceutical industry. I have extensive experience in the medical field. I have worked in the areas of study, including but not limited to, and the underserved.
  • organization, mentor, shipping, phlebotomy, hipaa, quality assurance, quality, training, vital signs, screening, staff training, clinical trial, clinical trials, iv, research, implementation, edc, sops, communication, fda, clinical, safety, coordinator, spirometry
  • phlebotomy, shipping, clinical trials, iv, recruitment, vital signs, clinical, coordinator, research
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Chevron Texaco

    • Conducted training and orientation of study staff, including but not limited to, protocol, informed consent, IRB, and regulatory requirements, SOP, CRF design, data collection, quality assurance, and adverse event reporting
    • Perform all aspects of clinical research including but not limited to protocol adherence, study start-up, safety, vital signs, drug accountability, source document verification, subject accountability, and regulatory documentation.
    • Conduct subject recruitment, informed consent, and HIPPA audits; perform clinical study procedures, including phlebotomy, specimen collection, and laboratory testing.
    • Perform all aspects of clinical trials including but not limited to: Protocol adherence, study initiation, study close-out, and IRB submissions.
    • Perform clinical research Coordinator duties as assigned, including but not limited to protocol preparation, informed consent process, subject safety, study close-out, and IRB submissions.
    • Participating in the initiation, monitoring and close out of clinical trials. Assist in the preparation of protocols, SOPs, and training manuals.
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Blue Cross Animal Hospital

    • Coordinator of the clinical trial, including recruitment, consenting, obtaining informed consent, and performing ECG's, blood draws, and ECGs.
    • Certified in phlebotomy, EKG, vital signs, and other research procedures. Perform all phases of study visits.
    • Perform ECGs, blood draws, and IV infusions for the study of patients. Collect and process specimens for shipment to sponsor.
    • Assist in the preparation of study documents for IRB approval and review. Ensure that all regulatory binders are followed.
    • Ensure that all study related documents are completed in a timely manner and in compliance with the protocol. Assist in the preparation of TMF.
    • Ensured that all study activities are conducted in accordance with the protocol, the study protocol, and the applicable regulatory requirements.


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