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Clinical Research Nurse (On-Call) /Madison, WI (On-Site)

Fortrea
Posted a month ago, valid for 18 days
Location

Madison, WI 53774, US

Salary

$33.85 - $40.63 per hour

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Contract type

Full Time

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Sonic Summary

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  • We are seeking a Clinical Research Nurse I (On-Call) to work in our Early Phase Clinical Research Units in Madison, WI, with a salary of approximately $50,000 per year.
  • The role requires 0-1 year of related experience and an Associate's or Bachelor's degree in nursing with current licensure.
  • You will interact with healthy volunteer participants, administer investigational compounds, and ensure their safety and well-being during clinical trials.
  • This fast-paced position involves adapting to changing priorities and requires strong teamwork and communication skills.
  • Candidates should be CPR/AED certified, with ACLS certification preferred, and must be comfortable working in a technology-based environment.

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 Clinical Research Nurse I (On-Call), to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, 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.)

This is a full-time, office/clinic-based job in Madison, WI.

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 this 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:

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.

Other key responsibilities:

  • Ensure that the dignity, health, safety, and welfare of participants is given the highest priority at all times

  • Be current with appropriate emergency certifications and company emergency policy and procedures

  • Respond to emergency situations based upon nursing standards

  • Utilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials

  • Utilize nursing assessment skills to observe participant general well-being and potential adverse events. Document adverse events and takes 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

  • Undertake any other duties as required

Education / Experience:

  • Associates Degree or BS degree in nursing with current licensure in applicable state.

  • CPR/AED certified

  • ACLS-certified preferred upon entry to role. ACLS certification maybe be gained in role if not yet certified

  • Additional experience may be substituted for education requirements

YOU NEED TO BRING…

  • 0-1 year of related experience

  • Additional experience may be substituted for education requirements

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.

Physical Requirements:

  • Ability to work in an upright and /or stationary position for 6-8 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.

Learn more about our EEO & Accommodations request here.




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