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Research Nurse I – Daytona Beach, Fl

2-3 years
Not Disclosed
10 Nov. 25, 2025
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

 Research Nurse I – Daytona Beach, FL
Location: Daytona Beach, Florida, USA
Category: Patient Services
Job ID: 251508
Employment Type: Full-time, Rotating Shifts, On-site

Overview:
Join one of the world’s leading Clinical Research Organizations (CROs) and play a key role in advancing early-phase clinical trials. Our Clinical Pharmacology Start-up team in Daytona Beach, FL is seeking a Research Nurse I to drive the initiation and execution of Phase 1 clinical trials with speed, accuracy, and patient-centered care.

This is an office and clinic-based position offering the opportunity to work closely with cutting-edge therapies in collaboration with top pharmaceutical, biotechnology, and medical device companies. You will contribute directly to establishing drug safety, tolerability, and pharmacokinetics, impacting patients globally.

Key Responsibilities:
As a Research Nurse I, your role will combine patient care, clinical expertise, and study execution. Responsibilities include:

  • Administer investigational compounds, including parenteral drugs, following protocol and regulatory guidelines.

  • Conduct nursing assessments, monitor participant well-being, and identify adverse events.

  • Obtain informed consent and educate participants on study procedures.

  • Perform clinical procedures including cannulation, telemetry, Holter monitoring, vital signs, ECGs, and venipuncture.

  • Collect and process biological samples in accordance with study protocols and SOPs.

  • Document study data accurately in Case Report Forms and electronic systems.

  • Respond to clinical emergencies using nursing standards and judgment.

  • Support a variety of study types including first-in-human, ascending dose, food effect, and drug-drug interaction trials.

  • Collaborate with study teams to ensure timely and protocol-compliant execution.

Requirements:

  • Associate’s or Bachelor’s degree in Nursing (BSN preferred) with active state licensure.

  • CPR/AED certification required; ACLS preferred.

  • Minimum 2–3 years of professional nursing experience, preferably in clinical research or patient care.

  • Strong clinical judgment, attention to detail, and ability to work in a fast-paced, protocol-driven environment.

  • Ability to work long shifts (10–12 hours), perform repetitive tasks, and lift up to 20 lbs as needed.

  • Comfortable working with technology and electronic data capture systems.

  • Flexibility to travel occasionally for site visits within the U.S.

Work Environment:

  • On-site clinical and laboratory setting with potential exposure to biological fluids.

  • Fast-paced environment with changing priorities requiring adaptability and teamwork.

  • Use of personal protective equipment (PPE) as required for safety.

Why Join Us:

  • Opportunity to contribute to early-phase clinical trials for innovative therapies.

  • Work closely with leading scientists, clinicians, and global pharmaceutical partners.

  • Full-time employees receive comprehensive benefits:

    • Medical, Dental, Vision, Life, STD/LTD insurance options

    • 401(k) retirement plan

    • Paid Time Off (PTO)

    • Employee recognition programs and resource groups

Apply Today:
Advance your clinical nursing career while impacting global healthcare. Join our team in Daytona Beach, FL, and be part of the innovation driving the next generation of therapies.


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