CLINICAL RESEARCH RN II

About the role

The Clinical Research Nurse II (CRN II) facilitates clinical research activity at Moffitt Cancer Center and/or affiliated institutions. They lead the coordination of opening new protocols, new patient evaluation, registering eligible patients, and coordinating protocol-related care of patients enrolled on clinical trials.

Responsibilities

• Facilitate clinical research activity by leading the coordination of opening new protocols, new patient evaluation, registering eligible patients, and coordinating protocol-related care of patients enrolled on clinical trials.
• Lead the screening, enrollment, and follow-up of study subjects, ensuring protocol compliance and close monitoring while subjects are on study.
• Act as liaison between investigators, primary care providers, Moffitt regulatory staff, and the sponsor.
• Coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines.
• Maintain regulatory files in conjunction with the regulatory specialist, maintain subject accruals, and track protocols.
• Ensure data and source documentation, adverse experience reporting, and maintenance of regulatory files.

Requirements

• Bachelor of Science in Nursing (BSN) from an ACEN or CCNE accredited institution, with a current FL RN license and three (3) years of relevant nursing experience. Two of the three years must be direct research nursing experience.
• In lieu of BSN, an Associate Degree in Nursing (ADN/ASN) from an ACEN or CCNE accredited institution with a current FL RN license and five (5) years of relevant nursing experience. Two of the five years must be direct research nursing experience.
• An applicant for this position, who will be or is seeking Florida licensure by endorsement, must not have any National Practitioner Data Bank (NPDB) reports, unless the applicant has successfully appealed to have their name removed from the NPDB.

Qualifications

• Current Florida RN license.
• Three (3) years of relevant nursing experience, with two years being direct research nursing experience.
• Five (5) years of relevant nursing experience, with two years being direct research nursing experience.
• No National Practitioner Data Bank (NPDB) reports, unless the applicant has successfully appealed to have their name removed from the NPDB.

Skills

• Knowledge of protocol requirements and good clinical practices as set forth by Federal regulations.
• Ability to coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines.
• Experience acting as liaison between investigators, primary care providers, Moffitt regulatory staff, and the sponsor.
• Experience screening, enrolling, and following study subjects, ensuring protocol compliance and close monitoring.
• Experience with data and source documentation, adverse experience reporting, and maintenance of regulatory files.

Benefits

Moffitt Cancer Center offers competitive benefits packages that include health insurance, retirement plans, and paid time off. Employees also have access to wellness programs and professional development opportunities.

Pay

The salary range for the Clinical Research Nurse II (CRN II) position is not specified in the job posting. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.

Schedule

The schedule for the Clinical Research Nurse II (CRN II) position is not specified in the job posting. However, it is likely that the position involves regular office hours and may require occasional evenings or weekends depending on the needs of the clinical trials being conducted.