Clinical Trials Nurse Navigator

This is a fully remote position, open to applicants in Florida.

📋 Description

• Proactively evaluate the practice's patient demographic against current and upcoming trial protocols to pinpoint potential clinical trial candidates.

• Conduct eligibility assessments based on protocol-driven inclusion/exclusion criteria and highlight borderline cases for review by the physician/PI.

• Complete feasibility questionnaires and evaluations for sponsors and CROs.

• Assess incoming trial opportunities and contribute to developing a strong, diverse clinical trials portfolio that aligns with the practice's patient demographic and strategic objectives.

• Collaborate with treating physicians, research coordinators, regulatory personnel, and representatives from sponsors/CROs on trial initiation and patient identification processes.

• Ensure accurate, audit-ready records of screening, feasibility, and eligibility are maintained in accordance with GCP and practice standards.

• Monitor the open trial portfolio and pipeline, keeping current with protocol eligibility criteria.

• Carry out any additional duties as assigned.

⛳️ Requirements

• An active, unencumbered RN license in the state of practice is required.

• A multi-state/compact RN license is advantageous.

• A minimum of 2–3 years of experience in oncology nursing, including infusion, inpatient oncology, or oncology research.

• A solid understanding of oncology diagnoses, staging, treatment protocols, and relevant lab/imaging values for trial eligibility.

• Excellent written and verbal communication abilities.

• Experience in accurately completing detailed forms/questionnaires.

• Highly organized and self-motivated.

• Ability to manage a caseload independently in a remote setting.

• Proficiency in EMR systems and standard office/productivity software.

• Previous experience in clinical research, trial coordination, or feasibility assessments is preferred.

• Familiarity with GCP guidelines and IRB procedures is preferred.

• OCN, CCRP, or CCRC certification is preferred.

• Experience working directly with pharmaceutical sponsors or CROs is preferred.

🏝️ Benefits

• Full-time position, Monday–Friday.

• Remote-friendly work arrangement (80–100%).

• Salary commensurate with experience and qualifications.

• EEO Employer.

• Drug-Free Workplace.