Clinical Trials Nurse Navigator

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🐊 Florida – Remote

🐊 Florida – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

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Cancer Specialists of North Florida

WebsiteLinkedInAll Job Openings

201 - 500 employees

🏥 Healthcare

💊 Pharmaceuticals

🔬 Science

Healthcare • Pharmaceuticals • Science

Cancer Specialists of North Florida is a physician-owned oncology practice delivering comprehensive cancer care across multiple community locations in North Florida. The practice provides medical oncology and hematology, radiation oncology, diagnostic imaging, specialty pharmacy services, clinical trials, and supportive services such as counseling, nutrition, and financial coordination. They emphasize personalized, community-based care with experienced physicians, state-of-the-art technology, and a focus on patient-centered outcomes.

📋 Description

• Proactively screen the practice's patient population against open and upcoming trial protocols to identify potential clinical trial candidates • Conduct protocol-driven inclusion/exclusion eligibility reviews and flag borderline cases for physician/PI review • Complete feasibility questionnaires and assessments for sponsors and CROs • Evaluate incoming trial opportunities and help build a robust, diverse clinical trials portfolio aligned with the practice's patient population and strategic goals • Collaborate with treating physicians, research coordinators, regulatory staff, and sponsor/CRO representatives on trial start-up and patient identification pipelines • Maintain accurate, audit-ready screening, feasibility, and eligibility records in accordance with GCP and practice standards • Track the open trial portfolio and pipeline and maintain working knowledge of protocol eligibility criteria • Perform all other duties as assigned

🎯 Requirements

• Active, unencumbered RN license in the state of practice required • Multi-state/compact RN license is a plus • Minimum 2–3 years of oncology nursing experience in infusion, inpatient oncology, or oncology research • Strong understanding of oncology diagnoses, staging, treatment regimens, and lab/imaging values relevant to trial eligibility • Strong written and verbal communication skills • Experience completing detailed forms/questionnaires accurately • Highly organized and self-directed • Comfortable managing a caseload independently in a remote environment • Proficiency with EMR systems and standard office/productivity software • Prior clinical research, trial coordination, or feasibility assessment experience preferred • Familiarity with GCP guidelines and IRB processes preferred • OCN, CCRP, or CCRC certification preferred • Experience working directly with pharmaceutical sponsors or CROs preferred

🏖️ Benefits

• Full-time position, Monday–Friday • Remote-friendly work arrangement (80–100%) • Salary commensurate with experience and qualifications • EEO Employer • Drug Free Workplace