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Research Nurse - Early Phase Clinical Trials (Night Shift)

Fortrea
Fortrea
2-3 years
Not Disclosed
Daytona Beach, United States
10 Feb. 14, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Research Nurse – Early Phase Clinical Trials (Night Shift) | Daytona Beach, Florida

Location: Daytona Beach, Florida, United States
Job Category: Clinical Research / Patient Services
Employment Type: Full-Time (On-Site, Night Shift)
Experience Required: 2–3 years of nursing experience (Early Phase or Clinical Research preferred)

Shift Schedule

  • Monday–Friday: 10-hour night shifts, 9:00 PM – 7:00 AM

  • Weekends (as scheduled): 12-hour night shifts, 7:00 PM – 7:00 AM

  • Structured and predictable overnight rotations

About the Organization

Join Fortrea, a leading global Contract Research Organization (CRO) delivering clinical development and technology solutions across more than 20 therapeutic areas. With operations spanning approximately 100 countries and multiple Early Phase Clinical Research Units in the United States and United Kingdom, Fortrea plays a critical role in advancing innovative therapies from first-in-human trials through regulatory approval.

Position Overview

Fortrea is seeking a dedicated Research Nurse to support Early Phase (Phase I) clinical trials during overnight operations in Daytona Beach, Florida. This role is ideal for registered nurses who prefer night shifts, value schedule consistency, and want to build expertise in early drug development.

As a Night Shift Research Nurse, you will ensure participant safety, protocol adherence, and accurate clinical data collection during critical overnight study windows. You will work in a structured, compliance-driven environment focused on safety, tolerability, and pharmacokinetics of investigational therapies.

Key Responsibilities

  • Deliver high-quality nursing care to clinical trial participants in accordance with study protocols and regulatory standards

  • Monitor participant safety, document adverse events, and respond to emergency situations as required

  • Administer investigational products and perform study-related procedures, including ECGs, telemetry monitoring, and venipuncture

  • Collect, process, and document biological samples in compliance with protocol requirements

  • Maintain accurate electronic source documentation and ensure data integrity

  • Ensure informed consent compliance and adherence to ICH-GCP and FDA guidelines

  • Collaborate with physicians, research coordinators, and cross-functional teams to ensure smooth overnight trial execution

Required Qualifications

  • Associate’s or Bachelor of Science in Nursing (BSN preferred)

  • Active and unrestricted Registered Nurse (RN) license in the state of Florida

  • 2–3 years of clinical nursing experience (hospital, acute care, or critical care experience preferred)

  • Phlebotomy experience required

  • Current CPR/AED certification (ACLS preferred)

  • Strong clinical assessment skills and ability to work independently during overnight shifts

Preferred Qualifications

  • Experience in Early Phase (Phase I) clinical trials

  • Familiarity with clinical research protocols and electronic data capture systems

  • Experience in telemetry or high-acuity patient monitoring

Work Environment

  • Laboratory and clinical research unit setting

  • Exposure to biological fluids

  • Personal protective equipment (PPE) required, including protective eyewear, garments, and gloves

  • Occasional local travel to site locations

  • Technology-enabled environment utilizing electronic clinical systems

Physical Requirements

  • Ability to remain upright or stationary for 10–12 hours per shift

  • Repetitive hand movements for operating medical and laboratory equipment

  • Frequent bending, twisting, and occasional stooping

  • Ability to lift and carry up to 15–20 lbs

  • Consistent and reliable attendance with flexibility for scheduled night and weekend coverage

Work Environment Expectations

  • Fast-paced, protocol-driven clinical research setting

  • Strict adherence to study timelines and regulatory requirements

  • Ability to adapt to changing priorities in real time

  • Strong teamwork and communication skills

  • Fully electronic documentation and data collection systems

Compensation and Benefits

Employees working 20 or more hours per week are eligible for comprehensive benefits, including:

  • Medical, Dental, and Vision Insurance

  • Life Insurance and Short-Term/Long-Term Disability coverage

  • 401(k) Retirement Plan

  • Paid Time Off (PTO)

  • Employee Recognition Programs

  • Employee Resource Groups (ERGs)

Why Join Fortrea

This Night Shift Research Nurse opportunity offers predictable scheduling, specialized early-phase research exposure, and meaningful impact in drug development. You will contribute directly to first-in-human and early-stage clinical trials that establish the safety profile of future therapies.

Advance your clinical nursing career in early-phase research while maintaining structured overnight rotations that support work-life balance.

Apply now through ThePharmaDaily.com to join a global leader in clinical research and help shape the future of medicine.