Shannon Lloyd

Clinical Research Coordinator at University of Florida Jacksonville Physicians, Inc.
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Contact Information
us****@****om
(386) 825-5501

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Credentials

  • certified clinical research coordinator
    Association of Clinical Research Professionals
    Nov, 2008
    - Nov, 2024

Experience

    • United States
    • Hospitals and Health Care
    • 100 - 200 Employee
    • Clinical Research Coordinator
      • Mar 2021 - Present

  • Self-employed
    • Jacksonville, Florida Area
    • Business Owner
      • Nov 2015 - Feb 2021

    • United States
    • Research Services
    • 1 - 100 Employee
    • Certified Clinical Research Coordinator
      • Feb 2008 - Nov 2015

      • Worked in partnership with site principal investigator to oversee the ethical and accurate completion of all study procedures. • Reviewed financial objectives and in return created study budgets for each protocol. • Maintained all regulatory documents. • Maintained correspondence with sponsors, IRB and FDA. • Continued familiarity with FDA regulations for clinical research. • Screened potential study participants per given protocol. • Assessed patient condition and reported any significant variations from baseline measurements to Principal investigator. • Processed, dispensed and stored all test articles separately. • Preformed patient vitals, and ECGs. • Collected, processed and shipped patient lab specimens. • Gave direct patient education on study specific ailment or condition. • Developed appropriate patient education tools and appointment schedule for individual studies. • Addressed all patient adverse events and serious events in a timely manner. • Documented patient data on case report forms and sponsor approved source documents. • Attended and participated in investigator meetings, seminars and national research meetings. • Submitted accurate data for computer tracking. • Participated in all sponsor site visits. • Oversaw patient recruitment, retention and data collection for team protocols. • Attended weekly research meetings. • Assisted in research department employee training and development.

    • United States
    • Hospitals and Health Care
    • 100 - 200 Employee
    • Clinical Research Associate
      • Oct 2006 - Jan 2008

      • Assisted residents in creating and maintaining protocols, which were required for graduation. • Authored resident teaching manuals for protocol submission process. • Maintained regulatory documentation and patient charts. • Submitted study specific documentation to Institutional Review boards for approval and continuing review. • Kept open correspondence with FDA and study sponsors. • Executed daily chart review for open site protocols. • Prepared for sponsor visits. • Attended weekly local IRB meetings. • Attained, processed and packed patient laboratory specimens. • Assisted physicians with patient vitals, ECGs and gynecological exams. • Assisted Private investigator and sub investigators with subject research visits, • Maintained patient data base per HIPPA regulations. • Created patient advertising and education material. • Collaborated with site manager in creating study budgets and executing study specific contracts.

    • United States
    • Higher Education
    • 500 - 600 Employee
    • Clinical Research Assistant
      • Mar 2004 - Oct 2006

      • Assisted study coordinators with patient visits. • Maintained regulatory documentation. • Executed original submission of sponsor and PI generated protocols to the local and central IRBs. • Assisted providers in their research fellowship obligations. This included development of protocol, IRB approval, execution and publication. • Submitted protocol specific continuing reviews. • Attended weekly research meetings. • Assisted with subject questionnaires, vitals and ECGs. • Accompanied study coordinators to study specific Principal Investigator meetings.

Education

  • Florida State College at Jacksonville
    Bachelor of Science - BS
    2018 -

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