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Lab Sample Coordinator / Dallas, TX (On-Site)

Fortrea
Full-time
On-site
hybrid
Clinical Research and Development
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Lab Sample Coordinator / Dallas, TX (On-Site)

Company Name: Fortrea

Job Description

  • Shipping and/or warehouse experience strongly preferred***

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 Sample Lab Coordinator I 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 Dallas, TX.

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 Responsibilities

  • Prepare, label, store, pack and dispatch samples to external laboratories in accordance with federal regulations.
  • Learn and apply correct shipping procedures according to international regulations for biohazardous and dangerous goods.
  • Complete all related documentation. Tracks and documents PK sample shipments.
  • Organize and communicate sample dispatch dates.
  • Formulates specimen codes from protocol and prints labels.
  • Labels and sets up specimen containers.
  • Obtains body substances for testing in the approved manner. These substances may include blood, saliva, sputum, urine, and stool.
  • Uses universal precautions when handling specimens.
  • Assist with the maintenance, testing, calibration and cleaning of clinical equipment within the Clinical Operations department.
  • Monitor temperature and organize refrigerator and freezer space. Arrange for clinical samples to be archived as required.
  • Operates and maintains centrifuges, as required.
  • Perform basic laboratory procedures as appropriate.
  • 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.
  • 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.