Sarasota Memorial Health Care System
Location
Sarasota, Florida
Coordinates clinical trial activities, including regulatory submissions to the IRB and managing documentation compliance. Responsible for screening patients, facilitating informed consent, and performing sonography according to study protocols.
Requires a degree in Cardiovascular Technology and at least five years of healthcare experience with specific cardiac and vascular certifications. Must complete training in Good Clinical Practice and Human Subject Protection within 30 days of hire.
Prepares and submits regulatory submission to IRB and sponsors, documentation compliance for multiple study projects, audit preparation, and data submission. This position also will be responsible for advising patients of trial design, facilitating informed consent for investigators, following strict adherence to protocol procedures specific to each study, screening for possible trial patients, eligibility criteria, and patient follow up. This position is responsible for coordination of trial activities mentioned above, as well as, others.
Mandatory Education: AS: Associate of Science
Preferred Education: BD: Bachelor Degree
As part of Sarasota Memorial Health Care System’s commitment to keeping people safe, all individuals providing care to vulnerable populations are required to undergo background screening through The Florida Care Provider Background Screening Clearinghouse.
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