Clinical Research Technician II / Madison, WI (On-Site)

Fortrea•Madison, WI

10d•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. As a Clinical Research Technician II you will perform practical / administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements. This is a full-time, office based position in Madison, WI. Open to new grads and experienced clinical professionals. Includes six weeks of paid training. 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.

Requirements

High School Diploma or equivalent
0 – 1 year of related experience.
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.
Comfortable working in an environment with changing priorities constantly asking you to prioritize and adapt on the spot.
Teamwork and people skills are essential for the study to run smoothly.
Comfortable working in a technology based environment. We collect our data directly into an electronic environment.

Nice To Haves

EMT, Phlebotomy, CMA or CNA certification, preferred

Responsibilities

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.
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
Other duties as assigned