Shannon Lloyd
Clinical Research Coordinator at University of Florida Jacksonville Physicians, Inc.- Claim this Profile
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Bio
Credentials
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certified clinical research coordinator
Association of Clinical Research ProfessionalsNov, 2008- Nov, 2024
Experience
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University of Florida Jacksonville Physicians, Inc.
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United States
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Hospitals and Health Care
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100 - 200 Employee
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Clinical Research Coordinator
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Mar 2021 - Present
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Self-employed
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Jacksonville, Florida Area
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Business Owner
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Nov 2015 - Feb 2021
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Jacksonville Center for Clinical Research
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United States
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Research Services
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1 - 100 Employee
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Certified Clinical Research Coordinator
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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.
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University of Florida Jacksonville Physicians, Inc.
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United States
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Hospitals and Health Care
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100 - 200 Employee
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Clinical Research Associate
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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.
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University of Florida College of Medicine
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United States
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Higher Education
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500 - 600 Employee
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Clinical Research Assistant
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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.
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Education
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Florida State College at Jacksonville
Bachelor of Science - BS