Clinical Research Registered Nurse, Early Phase Clinical Trials - Daytona Beach, FL

Fortrea•Daytona Beach, FL

3d•Onsite

About The Position

As one of the largest Clinical Research Organizations in the world, we operate four Early Phase Clinical Research Units across the UK and US. We are seeking a dedicated Clinical Research Registered Nurse to support the execution of innovative Early Phase clinical trials, ensuring participant safety and protocol accuracy. This role is ideal for nurses who prefer rotating shifts, mid shift or night work, value schedule transparency, and thrive in a focused clinical research environment. Why You’ll Love This Role Clear Shift Structure: Work primarily 10‑hour shifts during the week, with extended 12‑hour coverage on weekends as needed—providing consistency while supporting critical study operations. Growth in Early Phase Research: Gain exposure to multiple therapeutic areas and first‑in‑human and early‑development studies, building specialized expertise in clinical research nursing. Purpose‑Driven Impact: Maintain hands‑on patient care while contributing directly to the development of future treatments during key overnight study periods. Your Impact: You'll collaborate with leading pharmaceutical, biotechnology, and medical device companies at a critical stage of clinical development - establishing the safety, tolerability, and pharmacokinetics of new drugs. You'll maintain direct participant interaction while witnessing the development of innovative therapies firsthand.

Requirements

Associate’s or BS degree in Nursing with current state licensure.
CPR/AED/ACLS certification.
Registered Nurse.
2–3 years of related experience.
Phlebotomy experience.
A passion for learning and adaptability to a structured rotating schedule.

Nice To Haves

Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Responsibilities

Deliver high-quality care to trial participants using your clinical judgment and nursing expertise.
Monitor participant well-being, document adverse events, and respond to emergencies.
Administer investigational compounds and perform study-related procedures (ECGs, telemetry, venipuncture, etc.).
Collect and process biological samples, maintain accurate records, and ensure compliance with protocols.
Other duties as assigned.