As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

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 Screening 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.)

This is a full-time, office/clinic-based job in Dallas, TX.

Work hours: Monday-Friday 7:00am-3:30pm. Occasionally may need to come a little earlier and stay later depending upon clinical trial needs.

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 Technicians 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:

• Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings.

• Preparation and accurate recording of ECGs/Holters.

• Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples.

• Monitors meals to ensure dietary compliance by research participants.

• Assist in the preparation of rooms and medical equipment.

• Assist with screening procedures as needed.

• Maintain a clean, safe and efficient working and study environment.

• Foster respectful relationships with study participants.

• Accurately record all research data obtained or observed.

• Assist with QC of source documents and case report forms.

• Maintains a basic understanding of current regulatory requirements.

• Attends all required meetings, as appropriate.

• Assist, as necessary, with study procedures.

• Maintains accurate records of all work undertaken.

• Maintains skills to perform all study tasks, as required.

• Maintains constant awareness of participant safety and dignity at all times.

• Handles participant complaints efficiently and effectively in order that their satisfaction is maintained.

• Ensures that client and participant confidentiality is maintained.

• Responds to client and team queries in a timely manner.

• Takes ownership for the quality and standard of own work.

• Observe study subjects for general well-being and report appropriately.

• Check in and check out study participants, as requested.

• All other duties as needed or assigned.

YOU NEED TO BRING…

• High School Diploma or equivalent

• EMT, Phlebotomy, CMA or CNA certification, preferred.

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)

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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