Research Nurse I - Daytona Beach, FL

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 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 full-time, rotating shift schedule, office / clinic-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…

Work Environment

Physical Requirements

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

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 :

Learn more about our EEO & Accommodations request here .