Clinical Research Technician, Early Phase Clinical Research - Dallas, TX

About this role

*** Please note that this role requires you have experience with taking vitals, blood draws and ECG's.***

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 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.

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, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you´ll touch many patient´s 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 ERG’s (employee resource groups)

Learn more about our EEO & Accommodations request here .

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