| Job Description: |
Work at UF research locations, across the greater Jacksonville area, prescreening, consenting, and enrolling participants in research studies, including inpatient at UFHealth Work closely with staff in the Institute for Population Health to determine study participant eligibility. Review eligibility and recruitment material; provide and explain enrollment information to research participants.
Must have independent transportation to travel to participating study clinics to conduct study visits, check-in visits, recruitment assistance and follow ups including functions necessary for successful completion of all protocol-required visits/procedures, such as vital signs, phlebotomy, diagnostic tests, dispensing of investigational product, scheduling, drug accountability/reconciliation, and organizational tasks as needed.
Coordinates and implements follow-up procedures to collect data from patient charts, medical records, interviews, questionnaires, and other sources.
Carefully review and understand the needs of each study
Report to the study Principal Investigator and IPH leadership on any participant adverse events (AEs) and serious adverse events (SAEs). Create and maintain source documents.
Work independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation. Submission of protocol, consent documents for IRB approval, and assist in preparing regulatory submissions as requested Process and ship Bio samples according to local and federal regulations
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| Preferred: |
Bachelor’s degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.
Experience in phlebotomy and clinical research is preferred. Excellent interpersonal skills and the ability to prioritize and effectively communicate verbally and in writing.
Bilingual (English and Spanish) ability.
Coordinates multiple tasks and works independently and productively in a fast-paced, deadline-oriented environment.
This position requires proficiency in data management and superior organizational skills.
Integrity, careful attention to detail; ability to maintain confidentiality, demonstrate professionalism and respect for subjects’ rights and individual needs; willingness to learn and maintain skills per HIPAA regulations and Good Clinical Practice guidelines.
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