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

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.

*** Work shift: Mon-Fri / 630am-230pm.

*** Open to new grads and experienced 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.

WHAT YOU WILL DO

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
• Other duties as assigned

YOU NEED TO BRING…

• High School Diploma or equivalent
• EMT, Phlebotomy, CMA or CNA certification, preferred
• 0 – 1 year of related 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.

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)

Physical Requirements:

• Ability to work in an upright and /or stationary position for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Regular and consistent attendance.
• Varied hours may be required.

Learn more about our EEO & Accommodations request here.