Fortrea logo

Laboratory Sample Coordinator (On-Call)

Fortrea

Madison, WIOnsitePosted 39 days ago
Part TimeEntry LevelResearch & ScientistCRO
Original posting ↗

Summary

Interact directly with 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.)

Job description

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.

What You Will Do

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

  • 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.

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.

Requirements

  • High School diploma or equivalent
  • Comfortable working in a fast-paced, team-oriented clinical environment
  • Ability to perform repetitive physical tasks
  • Regular and consistent attendance
  • Ability to work in an upright and/or stationary position for 6-8 hours per day
  • Repetitive hand movement to operate lab equipment
  • Occasional crouching, stooping, bending and twisting
  • Ability to access and use computer software
  • Light to moderate lifting up to 15-20 lbs

Company overview

Fortrea Holdings Inc. is a leading global contract research organization (CRO) that provides comprehensive clinical development solutions to the pharmaceutical, biotechnology, and medical device industries. Headquartered in Durham, North Carolina with operations in over 90 countries, Fortrea specializes in managing all aspects of clinical trials from Phase I through IV, including clinical pharmacology and post-approval services. The company offers a wide range of services including regulatory affairs, protocol design, operational planning, patient recruitment, project management, data management, biostatistics, pharmacovigilance, and medical writing. With over 30 years of clinical research experience, Fortrea has evolved from its heritage as Covance and Labcorp into a pureplay CRO focused on delivering agile, fit-for-purpose solutions for both emerging and established life sciences companies. The company has conducted more than 5,850 clinical trials involving over 1 million subjects in the past five years, with particular expertise in oncology, central nervous system disorders, rare diseases, and cell and gene therapies.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.