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

linical Pharmacology Start-up team and help initiate groundbreaking Early Phase clinical trials with speed and precision.

Why You’ll Love This Role
• Structured Rotations: Work consistent shifts for two weeks at a time before rotating—giving you predictable scheduling and time to plan your life.
• Variety Without Chaos: Experience different shifts and responsibilities while maintaining stability in your routine.
• Skill Growth: Exposure to diverse therapeutic areas and study types keeps your work engaging and helps you build expertise.
• Impactful Work: Stay connected to patient care while contributing to the development of life-changing treatments.

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.

What You Bring
• Associate’s or BS degree in Nursing with current state licensure.
• CPR/AED certification (ACLS preferred).
• 2–3 years of nursing experience.
• Phlebotomy experience.
• A passion for learning and adaptability to a structured rotating schedule.

Join us and enjoy a role where stability meets variety—predictable two-week rotations that keep your life organized 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.