PRN Research Nurse, Daytona Beach, FL

Fortrea; Daytona Beach (FL); On-site; USD 60,000 - 80,000; Part time

Job summary

Fortrea is seeking a PRN Research Nurse in Daytona Beach, FL, to support Clinical Pharmacology trials. This role involves providing care, conducting clinical assessments, and working closely with participants on cutting-edge medical technologies. A successful candidate will have nursing experience, current licensure, and will thrive in a fast-paced clinical environment.

Benefits

Medical, Dental, Vision, Life, STD/LTD

401(K)

Paid time off (PTO)

Employee recognition awards

Qualifications

• 2-3 years of nursing experience required.
• CPR/AED certified; ACLS preferred.
• Current nursing licensure in applicable state.

Responsibilities

• Provide high standard of care for clinical trial participants.
• Document adverse events and administer investigational compounds.
• Educate participants on study procedures.

Skills

Clinical judgement

Nursing assessment

Emergency response

Patient care

Research documentation

Education

Associate’s or BS degree in nursing

Job description

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As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.

We are currently seeking a PRN Research Nurse, to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical trials for our clients with maximum speed and efficiency.

This is a casual/PRN, office-based position in Daytona Beach, FL.

If you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability, and pharmacokinetics of a new drug.

Many Nurses are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.

What You Will Do

Learn. And grow. No two days will be the same; and this is because in the clinic you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.).

Other Key Responsibilities

• Utilize your skills, knowledge, nursing diagnosis, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon nursing standards.
• Utilize your nursing assessment skills to observe participant general well-being and potential adverse events.
• Document adverse events and take appropriate action as needed.
• Obtain Informed Consent and continue the ICF process by educating, explaining, and informing participants of study procedures.
• Administer investigational compounds (inclusive of parenteral) to participants according to the protocol and applicable regulations.
• Perform study related activities such as cannulation, telemetry, holters, vital signs, ECGs, venipuncture.
• Collect and process biological samples according to the study protocol and Standard Operating Procedures.
• Record data obtained in a timely, error free manner according to the protocol and Standard Operating Procedures, transcribing source data onto the Case Report Form.
• Other duties as assigned.
  
  

YOU NEED TO BRING…

• Associate’s degree or BS degree in nursing with current licensure in applicable state.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• CPR/AED certified.
• ACLS certified preferred.
• 2-3 years of nursing experience.
  
  

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?

Benefits

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.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Part-time

Job function

• Job function

  Health Care Provider

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