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

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:

• 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.