CLINICAL RESEARCH RN II -- MOFFITT INTERNATIONAL PLAZA

Moffitt Cancer Center

91d

About The Position

The Clinical Research Nurse II (CRN II) facilitates clinical research at Moffitt Cancer Center and affiliated institutions. The role leads coordination of new protocol openings, evaluates new patients, registers eligible patients, and coordinates protocol-related care for patients enrolled in clinical trials. The CRN II serves as a primary protocol resource and applies an in-depth knowledge of protocol requirements and good clinical practices under federal regulations. The CRN II coordinates and provides direct patient care, performs ongoing assessments, delivers patient education, and documents care according to standards and regulatory guidelines for research patients enrolled in Moffitt-run clinical trials. Working with investigators, the nurse screens, enrolls, and follows study subjects, ensuring protocol compliance and close monitoring. The CRN II also serves as a liaison among investigators, primary care providers, Moffitt regulatory staff, and sponsors, and manages study data and source documentation, adverse experience reporting, regulatory files with the regulatory specialist, subject accruals, and protocol tracking.

Requirements

For the BSN pathway: a BSN from an ACEN- or CCNE-accredited institution, a current Florida RN license, and three years of relevant nursing experience, including two years of direct research nursing experience.
Alternatively, an ADN/ASN in nursing from an ACEN- or CCNE-accredited institution, a current Florida RN license, and five years of relevant nursing experience, including two years of direct research nursing experience.
Applicants seeking Florida licensure by endorsement must not have any National Practitioner Data Bank (NPDB) reports unless they have successfully appealed to have their name removed from the NPDB.
In-depth knowledge of protocol requirements and good clinical practices under federal regulations.

Responsibilities

Coordinate the opening of new protocols.
Evaluate new patients and register eligible patients.
Coordinate protocol-related care for patients enrolled in clinical trials.
Coordinate and provide direct patient care, perform ongoing assessments, and deliver patient education.
Document care in accordance with standards and regulatory guidelines.
Serve as a liaison among investigators, primary care providers, Moffitt regulatory staff, and the sponsor.
Screen, enroll, and follow study subjects with the investigator, ensuring protocol compliance and close monitoring.
Maintain data and source documentation.
Report adverse experiences.
Maintain regulatory files in conjunction with the regulatory specialist.
Maintain subject accruals and protocol tracking.