Screening Technician, Early Phase Clinical Research - Dallas, TX

Fortrea•Dallas, TX

1d•Onsite

About The Position

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 Coordinators 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 clinical research.

Requirements

Bachelor’s degree, or MA certification and 2 years related experience. Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
1 year experience in a medical clerical role.

Responsibilities

Review study protocols to determine screening requirements and eligibility criteria.
Coordinate special screening needs with Study Managers and Recruitment leadership.
Ensure recruiting questionnaires accurately assess participant eligibility.
Prepare and manage screening and physical exam materials, including consent forms and medical histories.
Obtain informed consent and conduct required screening procedures (e.g., vitals, ECGs, spirometry, lab work).
Review, verify, and maintain accurate screening charts and lab results.
Track participant status and screening activities in the database.
Coordinate screening schedules, resources, and daily appointments with Clinical Operations.
Support Screening Reception, including volunteer tracking and payments.
Assist with training new screening staff as needed.
All other duties as needed or assigned.