CLINICAL RSCH INFUSION RN I

Moffitt Cancer Center
•$37 - $55

About The Position

The Clinical Research Infusion RN I delivers individualized, quality nursing care to patients participating in clinical trials and their families, following hospital guidelines, nursing practice standards and policies, the ANA Code of Ethics, and applicable regulatory requirements. The nurse provides personalized, patient- and family-centered care in alignment with Moffitt Nursing’s mission and professional practice frameworks. The role facilitates clinical research activity by performing ongoing assessments, educating patients, administering nursing care and protocol-related therapy, monitoring patients, and documenting care to support clinical-trial protocol compliance. The nurse maintains working knowledge of protocol requirements and good clinical practices and interacts with investigators, primary care providers, research staff, mid-level providers, and sponsors. The Clinical Research Unit supports clinical investigations by monitoring patients and administering investigational agents in an outpatient setting. At the McKinley location, the unit sees 40 to 80 patients daily and provides 30 to 60 investigational treatments, which may last from 15 minutes to 12 hours.

Requirements

  • A BSN from an accredited institution and at least one year of relevant experience, or an ASN from an accredited institution and at least two years of relevant experience.
  • Florida RN license.
  • BLS certification.
  • Applicants seeking Florida licensure by endorsement must not have National Practitioner Data Bank reports unless they have successfully appealed to have their name removed from the NPDB.

Responsibilities

  • Identify and document patients’ learning needs and provide patient education based on those needs.
  • Facilitate clinical research activity through ongoing patient assessments, nursing care, protocol-related therapy, patient monitoring, education, and documentation for patients enrolled in clinical trials.
  • Support compliance with clinical-trial protocols and applicable good clinical practice and regulatory requirements.
  • Interact with investigators, primary care providers, Moffitt research staff, mid-level providers, and sponsors.
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