Screening Technician / Dallas, TX (On-Site)

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 Technician 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.

Requirements

Must possess previous experience as a Medical or Screening Technician or as a Nursing Assistant.
Phlebotomy experience required
High School Diploma or equivalent
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.

Nice To Haves

Prior clinical research experience preferred
EMT, Phlebotomy, CMA or CNA certification, preferred.

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.