Clinical Research Nurse (Oncology) - 256650

Must Haves: Active Florida RN license, at least 1+ year of oncology experience, experience accessing ports, experience with oral IP dosing, clinical research experience preferred

Hours: Monday to Friday, 8am-4:30pm (start time of 7:15am for extended trial days, hourly role with occasional overtime). Every 8th Friday, able to leave early around 2pm EST.

Benefits: Full benefit package offered, medical, dental, vision, 401k, PTO, growth opportunities, etc.

Responsibilities

• 75% administrative / 25% patient-facing coordinating Phase I oncology trials; hands-on skills required for IV/port access and oral IP dosing.
• Coordinators must enjoy reading and learning complex protocols, as early-phase studies have strict, heavy requirements.
• Fast turnaround is required-if a patient was hospitalized, the CRC must write and submit the SAE report within 24 hours.
• The nurse must manage frequent disruptions (e.g., a PI walking in, an infusion room reaction, or a patient going off-study unexpectedly) without getting overwhelmed when days of prep work change instantly.
• Managing all appointment logistics for a caseload of 18–22 patients. This includes scheduling/coordinating blood transfusions, diagnostic scans, and off-site specialty visits (such as required ophthalmology appointments).
• While PIs handle the initial primary consent, the CRC is responsible for executing all re-consents whenever study updates come down from sponsors
• Ensuring all patient medical records are gathered and on file (though ~90% come internally)

Required Skills

• Active FL RN license
• At least one year of recent experience working in Oncology as a RN