What are the responsibilities and job description for the Lab Sample Coordinator, Early Phase Clinical Research - Dallas, TX position at Fortrea?
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, Monday - Friday with occasional weekends, office-based position in Dallas, TX.
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:
What You Bring
This is a full-time, Monday - Friday with occasional weekends, office-based position in Dallas, TX.
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.
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 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.
- 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.
- 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.
- 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)