Lab Sample Coordinator, Early Phase Clinical Research – Dallas, TX

Fortrea

  • Dallas, Texas
  • 3 days ago
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    Skills

    • Calibrationunmatched
    • Centrifugeunmatched
    • Cleaning Equipmentunmatched
    • Clinical Laboratoryunmatched
    • Clinical Researchunmatched
    • Clinical Trialunmatched
    • Computer Softwareunmatched
    • Data Collectionunmatched
    • Detail Orientedunmatched
    • Electrical Componentsunmatched
    • Insuranceunmatched
    • Laboratory Equipmentunmatched
    • Laboratory Techniquesunmatched
    • Laptop PCunmatched
    • Lift/Move 20 Poundsunmatched
    • Office Equipmentunmatched
    • Operational Supportunmatched
    • Order Picking/Packingunmatched
    • Organizational Skillsunmatched
    • Regulationsunmatched
    • Research Protocolsunmatched
    • Software Developmentunmatched
    • Specimens/Samplesunmatched
    • Team Playerunmatched
    • Time Managementunmatched

    Description

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

    Join one of the world’s largest Clinical Research Organizations and contribute to early‑phase clinical trials that help bring new therapies to life. As a Sample Lab Coordinator I, you’ll support healthy volunteer studies and ensure accurate handling, tracking, and shipment of clinical samples in a fast‑paced, team‑oriented environment.

    This is a full-time, office-based position in Dallas, TX, working Monday through Friday. To support operational needs and provide scheduling flexibility, shifts may be scheduled 9:00 AM–5:30 PM or 10:00 AM–6:30 PM. Candidates should be comfortable working within these varying start times and thrive in a collaborative, fast-paced environment.

    What You’ll Do

    In this role, you’ll play a vital part in the sample management process for Phase 1 clinical studies. Key responsibilities include:

    • Preparing, labeling, storing, packing, and shipping samples to external labs.

    • Learning and following international shipping regulations for biohazardous materials.

    • Completing all required documentation and tracking PK sample shipments.

    • Organizing dispatch schedules and communicating timelines.

    • Setting up and labeling specimen containers.

    • Collecting approved body substances (e.g., blood, saliva, urine) using proper precautions.

    • Operating and maintaining centrifuges and other lab equipment.

    • Monitoring temperatures, organizing storage space, and achieving samples.

    • Supporting routine equipment cleaning, calibration, and basic lab procedures.

    You’ll gain exposure to innovative therapies and play a key part in clinical studies that impact patients worldwide. This role offers hands‑on experience in clinical research and the opportunity to grow within a global organization.

    What You Bring

    • High school diploma or equivalent.

    • Shipping and/or warehouse experience or logistics strongly preferred.

    • Ability to thrive in a fast‑paced, regulated clinical environment.

    • Strong attention to detail and teamwork skills.

    Work Environment:

    • Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

    • Occasional drives to site locations, occasional domestic travel.

    • Exposure to biological fluids.

    • Personal protective equipment required such as protective eyewear, garments, and gloves.

    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.

    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?

    • 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.

    Numbers & Facts

    LocationDallas, Texas
    Websitecareers.fortrea.com/us/en/eeo-and-accommodations

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