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

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Fortrea

Daytona Beach, Florida

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.

Posted Sep 23 · 2 years of experience

Shift and hours
Rotating shifts · 10-⁠hour shifts · Mid shift starting 11am–1pm · Night shift, 9pm-7:30am · Monday-Friday 10-⁠hour shifts · 12-⁠hour weekend nights, 7pm-7:30am
Unit and setting
Tele · Clinical Research
License
RN license Associate’s or BS degree in Nursing with current state licensure.Current state licensure
Term
Permanent

Do you qualify?

License
Current state licensure Associate’s or BS degree in Nursing with current state licensure.
Certification
CPR/AED/ACLS certification CPR/AED/ACLS certification.
Education
Associate’s or BS in Nursing
Experience
2-3 years of related experience 2-3 years of related experience.
Experience
Phlebotomy experience Phlebotomy experience.
Also asks
Adaptability to a structured rotating schedule A passion for learning and adaptability to a structured rotating schedule.

What it pays

Eligibility
Benefits for employees working 20+ hours per week Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:Working 20 or more hours per week

Benefits

  • BenefitsMedicalMedical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • BenefitsDental
  • BenefitsVision
  • BenefitsLife
  • BenefitsSTD/LTD
  • BenefitsPaid time off (PTO)Paid time off (PTO)
More benefits (9)
  • BenefitsEmployee recognition awardsEmployee recognition awards
  • BenefitsMultiple ERG’s (employee resource groups)Multiple ERG’s (employee resource groups)
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Life insurance
  • STD/LTD insurance
  • 401(k)
  • Employee resource groups (ERGs)

The role and schedule

Day to day
Deliver high-quality care to trial participants Deliver high-quality care to trial participants using your clinical judgment and nursing expertise.
Day to day
Monitor participant well-being Monitor participant well-being
Day to day
Document adverse events document adverse events
Day to day
Respond to emergencies respond to emergencies
Day to day
Administer investigational compounds Administer investigational compounds
Day to day
Perform study-related procedures (ECGs, telemetry, venipuncture, etc.) perform study-related procedures (ECGs, telemetry, venipuncture, etc.)
Day to day
Collect and process biological samples Collect and process biological samples
Day to day
Maintain accurate records maintain accurate records
Day to day
Ensure compliance with protocols ensure compliance with protocols
Day to day
Other duties as assigned Other duties as assigned.
Cross-training
Exposure to multiple therapeutic areas Gain exposure to multiple therapeutic areas and first-in-human and early-development studies
Weekends
Rotating weekends including a 12-hour shift Rotating weekends to include a 12-hour shift
Travel
Occasional site drives and domestic travel Occasional drives to site locations, occasional domestic travel.
Details
Work in a laboratory and/or clinical environment Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
Details
Exposure to biological fluids Exposure to biological fluids.
Details
Protective eyewear, garments and gloves required Personal protective equipment required such as protective eyewear, garments and gloves.
Details
Upright and/or stationary 10-12 hours per day Ability to work in an upright and /or stationary position for 10-12 hours per day.
Details
Maximum lift 15-20 lbs Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Details
Varied hours may be required Varied hours may be required.
Details
Fast-paced; no protocol deviations allowed Fast paced : where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
Details
Changing priorities and on-the-spot adaptation Changing priorities constantly asking you to prioritize and adapt on the spot.
Details
Data collected directly into an electronic environment We collect our data directly into an electronic environment.

The workplace

Fortrea logo
Fortrea
Hiring organization

Worth asking

  • Can you walk me through base pay range and differentials?
  • What should I expect for weekly hours, holiday, and call?
More questions to ask
  • What orientation, preceptor time, and ongoing unit support are included?
  • How are patient load, floating, and staffing support handled day to day?
Build questions for this role

Your fit

On your path

Telemetry One of the most open front doors in acute care; ACLS and rhythm.

Original listing

Read full text

Clinical Research Registered Nurse - Early Phase Clinical Trials (Multiple Shifts Available)

Location: Daytona Beach, FL

Schedule Options

Option 1: Rotating Shift

  • 10-hour shifts
  • Rotating weekends to include a 12-hour shift

Option 2: Mid Shift

  • 10-hour shifts
  • Start time between 11am and 1pm
  • Rotating weekends to include a 12-hour shift

Option 3: Night Shift

  • Monday–Friday: 10‑hour shifts
  • 9pm - 7:30am
  • Rotating weekends to include a 12-hour shift (7pm - 7:30am)

Meaningful work. A chance to shape the future of medicine—while the world sleeps.

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.

What You’ll Do

  • 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.

What You Bring

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

Join us and enjoy a role where consistency meets purpose—structured shifts that support work‑life balance while you help shape the future of medicine.

Work Environment

  • Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
  • Occasional drives to site locations, occasional domestic travel.
  • Exposure to biological fluids.
  • Personal protective equipment required such as protective eyewear, garments and gloves.

Physical

Requirements

  • Ability to work in an upright and /or stationary position for 10-12 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

The important thing for us is you are comfortable working in an environment that is:

  • Fast paced : where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based . We collect our data directly into an electronic environment.

What do you get?

Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO)
  • Employee recognition awards
  • Multiple ERG’s (employee resource groups)

Learn more about our EEO & Accommodations request here .

What's around it?

In Daytona Beach, FL

Daytona Beach, FLFrom Census ACS 2024.

Living costs about the same as the US average

Median rent
$1,328/mo
Household income
$52,058/yr, all local households, not nurse pay

See Daytona Beach, FL

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