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Licensed as a Registered Nurse (RN) in the State of Florida. JOB SUMMARYThe Research RN, NCHRI works directly with the physician in accurately and professionally executing all clinical research projects in an acute care/inpatient setting (ED, Cath Lab, ICU, EP lab, Step down and OR) as well as the ambulatory and ancillary areas.
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The Research RN must possess the knowledge and clinical experience to work in many different areas with numerous teams in order to experience success in this position. NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Protocol driven research tasks performed by the physician are guided by the Research Nurse to assure all required steps are completed and performed in the correct order. · Provides nursing knowledge and decision-making support to non-RN research team members seeking support.
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Performs required procedures and data collection activities at necessary in observational settings such as, ED, Cath Lab, EP Lab, ICU/Step down area, physician office, OR, and other required areas. Advanced Life Support (ALS) certification preferred from the American Red Cross or American Heart Association.
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Assists screeners with patient consenting and performs re-consenting when necessary and in accordance with GCP. · Knows and fulfills IRB/FDA expectations in the execution of these critical tasks. Basic Life Support (BLS) certification required from the American Red Cross or American Heart Association.
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Serves as an internal and external resource for questions referencing clinical research at NCH. · Professionally represents Principal Investigator and NCH Research Institute at protocol meetings and conference calls in the absence of the Investigator.
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Guides referring physicians in GCP compliance and clinical care through protocol design and awareness through education. Coordinates critical research tasks and patient activities in accordance with Good Clinical Practice (GCP.
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EDUCATION, EXPERIENCE AND QUALIFICATIONS· Minimum of 2 years of experience in Critical Care/Cardiology preferred. Serves as the primary clinical trial contact person for study sponsor, patient, family, or other healthcare contacts or departments.
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Works with sponsor’s auditor/monitor to review and verify accuracy and completeness of data recorded. Oversees clinical research studies, collecting all clinical data in an accurate and timely manner.
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Facilitates physician oversight of all data, especially adverse event reporting as it relates to study drug, device, or therapy. Assures all data points are supported by medical records, physician notes, diagnostic reports, procedural summaries, or research project documents.
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Represents the Research Institute in a professional manner, demonstrating knowledge and enthusiasm for clinical research. Verifies that patients are scheduled appropriately for follow up evaluations per protocol.
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Our healthcare system is comprised of two hospitals, an alliance of 700+ physicians, and medical facilities in dozens of locations throughout Southwest Florida that offer nationally recognized, quality health care.
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