PRN Research Technician I - Dallas, TX at Fortrea
Dallas, TX 75247, USA -
Full Time


Start Date

Immediate

Expiry Date

28 Nov, 25

Salary

0.0

Posted On

28 Aug, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Technology

Industry

Pharmaceuticals

Description

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 PRN Research Technician, to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical trials for our clients with maximum speed and efficiency.
This is a casual, office-based position in Dallas, TX. Multiple openings.
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.

PREVIOUS CLINICAL EXPERIENCE IS IDEAL, BUT NOT A MUST. WE ARE OPEN TO CONSIDER RECENT GRADUATES OR ANY RECENT CLINICAL EXPERIENCE.

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.

How To Apply:

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Responsibilities

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

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.
  • Undertake any other duties as required.
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