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University of South Florida

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Nurse/Researcher (Finance)



This position typically reports to a physician faculty member that serves as the Principal Investigator (PI) of the research project or on rare occasions to an appropriate program administrator within the department. As the Study Coordinator for a research project, the Nurse Researcher oversees patient-related study activities, research regulatory compliance, data gathering and management according to Federal requirements, and ensures safe collection and preparation of blood and body fluids, including transportation of same. Most studies are grant funded, although a few are state, local and privately funded. Others are funded by pharmaceutical companies. Grant-funded projects involving human subjects require compliance with numerous stringent Federal, State, university, and department policies, procedures, rules and regulations, for which this position must know, interpret, comply, and prepare reports. Work at this level meets the FLSA criteria for a professional exemption since the primary duties require advanced knowledge which is predominantly intellectual in character and require the consistent exercise of discretion and judgment. Nurse Researchers differ from non-exempt nursing or research support staff in that the incumbents in these positions develop techniques and oversee clinical data gathering, establish quality control standards, develop educational materials, and serve as liaisons with regulatory agencies. The Principal Investigator sets the overall project direction and has responsibility for final interpretation of project results, but this position serves as a right-hand to the PI and provides input into the process.This position requires licensure as a registered nurse in accordance with Chapter 464, Florida Statutes, or eligible to practice nursing in accordance with Chapter 64 B9, Florida Administrative Code. Bachelor's degree in Nursing with two years of nursing research or directly related experience; OR an Associate's degree in Nursing with four years of same experience. A Master's degree in Nursing is Preferred. Annual certifications may be required to participate in specific studies.Working at USF
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With approximately 16,000 employees, the University of South Florida is one of the largest employers in the Tampa Bay area. We are dedicated to cultivating a talented, engaged and driven workforce that strives to be bold. Employees excel in USF's rich academic environment, which fosters their development and advancement. In 2025, Forbes recognized USF as one of Florida's best large employers, ranked No. 1 among the state's 12 public universities. Our first-class benefits package includes medical, dental and life insurance plans, retirement plan options, employee and dependent tuition programs, generous leave, and hundreds of employee perks and discounts.
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About USF
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The University of South Florida is a top-ranked research university serving approximately 50,000 students from across the globe at campuses in Tampa, St. Petersburg, Sarasota-Manatee and USF Health. USF is recognized by U.S. News & World Report as a top 50 public university and the best value in Florida. U.S. News also ranks the USF Health Morsani College of Medicine as the No. 1 medical school in Florida and in the highest tier nationwide. USF is a member of the Association of American Universities (AAU), a group that includes only the top 3% of universities in the U.S. With an all-time high of $738 million in research funding in 2024 and as a top 20 public university for producing U.S. patents, USF uses innovation to transform lives and shape a better future. The university generates an annual economic impact of more than $6 billion. USF's Division I athletics teams compete in the American Athletic Conference. Learn more at www.usf.edu .
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Compliance and Federal Notices
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This position may be subject to a Level 1 or Level 2 criminal background check.
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Applicants have rights under Federal Employment Laws :
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Family and Medical Leave Act (FMLA)
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Applicants for USF employment are entitled to request reasonable accommodation(s) in the application process. A request is to be made at least five (5) working days prior to the time the accommodation(s) is needed. Visit the Central Human Resources ADA Accommodations webpage for more information on requesting an accommodation during the application/interview process.
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  • Evaluates potential research participants with Principal Investigator; schedules screening evaluations; explains consent process; performs required screening evaluations; randomizes participants into appropriate research study.
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  • Coordinates and schedules study visits and follow-ups. Oversees or performs required procedures for each visit.
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  • Records data on each study participant for each visit according to research protocol, maintaining complete study progress notes and case report form for each visit.
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  • Reports any Adverse Events according to protocol. Communicates questions, problems, changes to the Principal Investigator.
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  • Prepares and submits protocol applications, amendments, annual reviews, Adverse Event reports, and study sponsor communications to IRB as required.
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  • Participates in specialty clinic, coordinating with clinic staff and physicians to evaluate patients that might be considered for research studies. Provides training and guidance in specialty area to patients and staff.
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  • Collects, analyzes, and performs quality assurance of study data. Monitors overall clinical study to insure that quality control measures are in compliance with protocol.
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  • Actively participates in research study meetings to discuss progress/status of study. Ensures consistent interpretation and adherence to protocols at all stages of trials by team members. Recommends changes in protocols to improve quality of data gathering or overall study.
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  • Ensures that Monthly, quarterly, annual and end of grant reports are completed and submitted to regulatory and granting agencies as required.
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  • Oversees the ordering, dispensing and maintenance of supplies and medications for the research study.
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  • Performs procedures as necessary, such as venipuncture, electrocardiograms, quantitative Sensory Testing, insulin testing, etc. for the study.
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  • Collaborates in development of new research grants, providing clinical nursing consultation in the development of protocols, research instrument design, coding and analysis, and selection of assessments. Assists in developing proposals for new research projects.
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  • May serve as an advocate for a specific population by participation in community fairs, programs, committees; state and national committees, programs and conferences.
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