Clinical Research Nurse I - Early Therapeutics

Moffitt Cancer Center

41d • $37 - $57

About The Position

The Clinical Research Nurse I (CRN I) facilitates clinical research activity at Moffitt Cancer Center and affiliated institutions. The role coordinates the opening of new protocols, evaluates new patients, registers eligible patients, and coordinates protocol-related care for patients enrolled in clinical trials. The nurse must have an in-depth understanding of protocol requirements and good clinical practices under federal regulations.

Serving as a primary resource for assigned protocols, the CRN I coordinates and provides direct patient care, performs ongoing assessments, educates patients, and documents care according to applicable standards and regulatory guidelines. In collaboration with investigators, the nurse screens, enrolls, and follows study subjects, ensuring protocol compliance and close monitoring. The role also serves as a liaison among investigators, primary care providers, Moffitt regulatory staff, and sponsors, and is responsible for data and source documentation, adverse experience reporting, regulatory file maintenance in conjunction with the regulatory specialist, subject accruals, and protocol tracking.

Requirements

• BSN from an ACEN- or CCNE-accredited institution with no experience required, or an ASN from an ACEN- or CCNE-accredited institution with 2 years of relevant experience.
• Florida RN license.
• Ability to plan, organize, and coordinate multiple work assignments.
• Ability to establish and maintain effective, collaborative working relationships.
• Ability to communicate clearly verbally and in writing.
• Applicants seeking Florida licensure by endorsement must not have NPDB reports unless they have successfully appealed to have their name removed from the NPDB.

Nice To Haves

• Direct research nursing experience.

Responsibilities

• Coordinate the opening of new protocols, new patient evaluation, registration of eligible patients, and protocol-related care for clinical trial participants.
• Coordinate and provide direct patient care, perform ongoing assessments, and deliver patient education.
• Document care in accordance with standards and regulatory guidelines.
• Screen, enroll, and follow study subjects in collaboration with investigators.
• Ensure protocol compliance and close monitoring of subjects while they are on study.
• Serve as a liaison among investigators, primary care providers, Moffitt regulatory staff, and sponsors.
• Maintain data and source documentation and report adverse experiences.
• Maintain regulatory files in conjunction with the regulatory specialist.
• Maintain subject accruals and protocol tracking.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level