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Screening Technician - Madison, WI (On-Site)
full-timeMadison

Summary

Location

Madison

Type

full-time

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About this role

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 Madison, WI.

Work hours: Monday-Friday 6:30am - 2:30pm CST.

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 work with gets approved, you know you’ll touch many patients’ lives around the world.

WHAT YOU WILL DO:

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.

Other key responsibilities:

  • Perform vital signs, venipuncture, and ECG/Holter procedures.

  • Collect, process, and document biological samples.

  • Monitor dietary compliance and participant well‑being.

  • Prepare rooms, equipment, and support screening.

  • Maintain clean, safe environments and accurate records.

  • Assist with study procedures and document QC.

  • Ensure participant’s safety, dignity, confidentiality, and satisfaction.

  • Respond promptly to inquiries and uphold work quality.

  • Support participant check‑in/check‑out.

  • All other duties as needed or assigned.

YOU NEED TO BRING…

  • Associate degree or BS degree preferred.

  • 1-2 years' experience in patient care.

  • EMT, Phlebotomy, CMA or CNA certification, preferred.

Work Environment:

  • Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

  • Occasional drives to site locations, occasional domestic travel.

  • Exposure to biological fluids.

  • Personal protective equipment required such as protective eyewear, garments and gloves.

Physical Requirements:

  • Ability to work in an upright and /or stationary position for 10-12 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.

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.

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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)

Learn more about our EEO & Accommodations request here.

Other facts

Tech stack
Vital Signs,Venipuncture,ECG,Holter Procedures,Biological Sample Collection,Dietary Compliance Monitoring,Clinical Judgment,Patient Care,Teamwork,Technology Proficiency,Record Keeping,Safety Protocols,Communication Skills,Adaptability,Attention to Detail

About Fortrea

Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.
Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.
Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.
Together, exceptional is possible.
Learn more at Fortrea.com

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Biotechnology Research

What you'll do

  • You will utilize your skills and clinical judgment to provide high standards of care in clinical research. Key responsibilities include performing vital signs, venipuncture, and ECG procedures, as well as monitoring participant well-being and ensuring safety.

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Frequently Asked Questions

What does a Screening Technician - Madison, WI (On-Site) do at Fortrea?

As a Screening Technician - Madison, WI (On-Site) at Fortrea, you will: you will utilize your skills and clinical judgment to provide high standards of care in clinical research. Key responsibilities include performing vital signs, venipuncture, and ECG procedures, as well as monitoring participant well-being and ensuring safety..

Why join Fortrea as a Screening Technician - Madison, WI (On-Site)?

Fortrea is a leading Biotechnology Research company.

Is the Screening Technician - Madison, WI (On-Site) position at Fortrea remote?

The Screening Technician - Madison, WI (On-Site) position at Fortrea is based in Madison, Wisconsin, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Screening Technician - Madison, WI (On-Site) position at Fortrea?

You can apply for the Screening Technician - Madison, WI (On-Site) position at Fortrea directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Fortrea on their website.