Laboratory Sample Coordinator (On-Call) / Madison, WI (On-Site)

On-site

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Responsibilities

Organize and communicate sample dispatch dates.
Monitor temperature and organize refrigerator and freezer space.
Arrange for clinical samples to be archived as required.
Perform basic laboratory procedures as appropriate.
Prepare, label, store, pack and dispatch samples to external laboratories in accordance with federal regulations.

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 Lab Sample Coordinator (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.
Other duties as assigned YOU NEED TO BRING… High School diploma or equivalent 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.
Teamwork and people skills are essential for the study to run smoothly. Technology based .
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.
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.

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 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 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
Learn and apply correct shipping procedures according to international regulations for biohazardous and dangerous goods.
Formulates specimen codes from protocol and prints labels.
Obtains body substances for testing in the approved manner.