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Clinical Research Technician, Early Phase Clinical Research Dallas, TX

Fortrea


Job Location:

Dallas, TX - USA

Monthly Salary: Not provided by the employer
Posted: 13 August 2026 (30+ days ago)
Application Deadline: 10 November 2026
Vacancies: 1 Vacancy

Job Summary

*** Please note that this role requires you have experience with taking vitals blood draws and ECGs.***

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 Clinical Research Technician 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.).

Schedule Options:

Option 1: Mid Shift

  • 10-hour shifts

  • Start time between 11am and 1pm

  • Every other weekend required

OR

Option 2: Weekend Day Shift

  • 12-hour shifts

  • Friday Saturday and Sunday

  • 6am to 6:30pm

If you join us you will work with some of the worlds 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 have a close face-to-face relationship with participants and as you continue to practice your clinical skills and knowledge youll be involved with the latest medical technologies and treatments witnessing their development firsthand. When the drug you worked with gets approved you know youll touch many patients 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:

  • Review study protocols and eligibility criteria to support participant screening.

  • Coordinate special screening procedures with study and recruitment teams.

  • Assist with development and accuracy of participant eligibility questionnaires.

  • Prepare and organize screening consent medical history and study documentation.

  • Obtain informed consent and collect medical histories from participants.

  • Perform and/or coordinate protocol-required screening procedures and assessments.

  • Review screening records for accuracy completeness and compliance.

  • Prepare screening charts for physician and study manager review.

  • Maintain accurate participant status records within the study database.

  • Other duties as assigned.

YOU NEED TO BRING

  • High school diploma or equivalent

  • 1-2 years research experience may be substituted for education requirement.

  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

  • EMT Phlebotomy CMA or CNA certification preferred.

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 ERGs (employee resource groups)

Learn more about our EEO & Accommodations request here.


Required Experience:

IC


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