Fortrea

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

United States · Work style not stated · Casual

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About the role

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  • EmployerFortrea
  • LocationUnited States
  • Work styleWork style not stated
  • Employment typeCasual
  • Employer posted

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 Technician II, (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 an On-call, office/clinic-based job in Madison, WI.

Work shift: 8 or 10 hour shifts available ( am/mid-afternoon/night) per applicants availability. No weekends required. However, weekend shifts are available if extra hours are desired.

*** Open to new grads and experienced clinical professionals. Includes six weeks of paid training.***

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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 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:

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

Other key responsibilities:

  • Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings
  • Preparation and accurate recording of ECGs/Holters
  • Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples
  • Monitors meals to ensure dietary compliance by research participants
  • Assist in the preparation of rooms and medical equipment
  • Assist with screening procedures as needed
  • Maintain a clean, safe and efficient working and study environment
  • Other duties as assigned

YOU NEED TO BRING…

  • High School Diploma or equivalent
  • EMT, Phlebotomy, CMA or CNA certification, preferred
  • 0 – 1 year of related 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.

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.

Learn more about our EEO & Accommodations request here.

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At a glance

  • Employment typeCasual
  • Employer posted
  • Added to ROLIVA
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