Clinical Research Nurse - Early Phase Clinical Trials (First Shift) - Daytona Beach, FL

Fortrea•Daytona Beach, FL

About The Position

Join our clinical research team as a Research Nurse supporting Phase I clinical trials. This Monday-Friday, first‑shift role (7am - 3pm) offers a consistent schedule and the chance to work in a collaborative environment focused on participant safety and high‑quality study execution. What You’ll Do Provide high‑quality clinical care with a strong focus on participant safety. Monitor participants, assess for adverse events, and document findings accurately. Administer investigational products and obtain informed consent. Perform clinical procedures including: Phlebotomy and venipuncture Vital signs, ECGs, telemetry, holters Cannulation and sample collection/processing Record and verify study data per protocol and SOPs. Maintain readiness for emergency response. Support clinic flow, including occasional shift lead duties. What You Bring Associate’s or Bachelor’s degree in Nursing. Active RN license in applicable state. CPR/AED certified (ACLS preferred or can be obtained after hire). Phlebotomy/venipuncture experience required. 1 year of experience. A great opportunity for nurses looking to expand their skill set, gain research experience, and grow within a dynamic and supportive clinical team. 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. Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide. Follow us and stay updated about Fortrea on LinkedIn, Facebook, X, Instagram, YouTube and Glassdoor. At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

Requirements

Associate’s or Bachelor’s degree in Nursing.
Active RN license in applicable state.
CPR/AED certified (ACLS preferred or can be obtained after hire).
Phlebotomy/venipuncture experience required.
1 year of experience.

Responsibilities

Provide high‑quality clinical care with a strong focus on participant safety.
Monitor participants, assess for adverse events, and document findings accurately.
Administer investigational products and obtain informed consent.
Perform clinical procedures including: Phlebotomy and venipuncture Vital signs, ECGs, telemetry, holters Cannulation and sample collection/processing
Record and verify study data per protocol and SOPs.
Maintain readiness for emergency response.
Support clinic flow, including occasional shift lead duties.