Experience

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  Orlando Health

  • United States
  • Hospitals and Health Care
  • 700 & Above Employee

  • BMT & Cellular Therapy Coordinator

    • Jan 2024 - Present

    Nurse Coordinator for solid tumor cellular therapy patients.

  • Clinical Operations Supervisor

    • Aug 2022 - Jan 2024

    Clinical research Operations supervisor for Phase I clinical trials as well as oncology trials in hematology, genitourinary, gastrointestinal, Bone marrow and cellular therapies.

  • Clinical Research Lead

    • Mar 2022 - Aug 2022

    Clinical Research lead for oncology Phase I team, Hematology, genitourinary, gastrointestinal, bone marrow and cellular therapies

  • Clinical Research Coordinator II - Early Phase Oncology

    • Jan 2018 - Mar 2022

• 

  AdventHealth

  • Orlando, Florida

  • Clinical Research Nurse -Neuroscience institute

    • Jun 2012 - Jan 2018
    • Orlando, Florida

    Clinical Research Nurse •Responsible for conducting Phase II-Phase IV clinical studies according to FDA regulations and guidelines•Conducting studies accurately and in compliance with GCP guidelines•Responsible for determining patient eligibility and informed consenting of patients•Responsible for maintaining patient safety and reporting of adverse events to investigator/sponsor•Maintaining research data by completing Case report forms, entering data into electronic system, and answering queries•dispensing and administering medication•Meeting with monitors to review site data•Maintaining regulatory documentsNormal Pressure Hydrocephalus Program Coordinator •Responsibilities included:oContacting referrals and explaining program in detailoScheduling appointments for hospital stay and follow upoCreating and presenting patient outcomes to a multidisciplinary team at a monthly conferenceoContacting patients with test results post conference

• 

  Omega Research Consultants

  • Deland, Florida

  • Clinical Research Coordinator

    • Mar 2011 - May 2012
    • Deland, Florida

    Responsible for conducting clinical studies according to FDA regulations and guidelinesResponsible for maintaining patient safety and reporting of adverse events to investigator/sponsorDesigning and utilizing tools to conduct studies accurately and in compliance with GCPMaintaining regulatory documentsResponsible for determining patient eligibility and informed consenting of patientsMaintaining research data by completing Case report forms, entering data into electronic system, and answering queriesdispensing and administering medicationMeeting with monitors to review site dataDrawing study specific labs, processing labs, and preparing for shipment