Get a reply from this employer — a resume and cover letter tailored to exactly what they’re hiring for.
Sarasota Memorial Health Care System is seeking a Research Coordinator to prepare and submit regulatory submissions to IRB and sponsors, ensuring strict documentation compliance across multiple study projects.
The role includes coordinating audit activities, advising patients on trial design, and facilitating informed consent while screening for eligible participants and coordinating trial activities. Strong GCP knowledge and healthcare experience are required.
Research Institute
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.
A D: Associate's Degree
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. https://info.flclearinghouse.com/