John Fechtner - Clinical Research Coordinator Resume Simple
Highly motivated, detail-oriented professional with more than 15 years of experience in the healthcare industry. I am a self-starter, able to prioritize and complete multiple tasks in a fast paced environment.
  • injections, contracts, vitals, recruiting, telephone, safety, budgets, responsible, therapy, phlebotomy
  • vitals, fax, clinical trials, compliance, pulmonary function, patient, fda, telephone, responsible, phlebotomy, clinical
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    The University of Scranton

    • Assist with study procedures, including phlebotomy, vitals, and medication therapy. Provide patients with any necessary information.
    • Assist with the recruitment of subjects, screening of potential participants, and filing of study documents. Responsible for the preparation of IRB submissions and renewals.
    • Coordinate and manage all aspects of the study including: recruiting, screening, consenting, randomization, and educating patients.
    • Prepare and submit regulatory documents to IRB. Maintain study budget and invoices. Ensure proper invoicing of all subjects.
    • Maintain a high level of contact with patients, vendors, and physicians to ensure proper billing and collection of all study participants.
    • Ensured that all study related activities, including but not limited to, the informed consent, source document verification, patient contact, and subject safety.
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Saxon Mortgage

    • Perform ECGs, vital signs, patient history, EKG, pulmonary function test, and electrocardiograms. Maintain accurate and complete records of study visits.
    • Responsible for the collection, organization, and verification of all study data from source documents to electronic CRFs, ensuring compliance with good clinical practice (GCP), and SOP’s.
    • Maintain accurate records of all study activities. Perform source documentation for subject visits. Review and approve informed consent forms for clinical trials.
    • Assist the PI in the preparation of the study, including but not limited to, vital signs, blood draws, lab specimen collection, and processing of all signed consent forms.
    • Ensure all study related procedures are performed in accordance with protocol requirements, SOP’s, and FDA regulations. Complete and submit all required paperwork to the IRB.
    • Obtain vitals, telephone triage, fax, copy, scan, and file documents. Maintain all study files.

 Noncommercial Users Constituency 

 European Metrology