Clinical Research Technician II: Phase 1 Trials (Madison)

Fortrea; Madison (WI); On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Medical, Dental, Vision, Life, STD/LTD

401(K)

Paid time off

Employee recognition awards

ERGs

Job summary

Fortrea in Madison, WI is seeking a Clinical Research Technician II to perform clinical and administrative tasks for phase 1 studies in a fast-paced environment. You will support participants, collect vital signs, and assist with ECGs and sample handling under protocol guidance.

Open to new grads and experienced professionals; includes six weeks of paid training and a typical Mon-Fri 6:30am-2:30pm shift. This office-based role connects you with world-leading pharma and medical device sponsors.

Qualifications

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

Responsibilities

• Provide high standard of care for participants in clinical trials and respond to emergencies according to protocol and regulatory standards.
• Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings.
• Prepare and record ECGs/Holters accurately.
• Collect and process biological samples as specified in the protocol.
• Monitor meals to ensure dietary compliance by research participants.
• Assist in room and medical equipment preparation.
• Assist with screening procedures as needed.
• Maintain a clean, safe, and efficient working and study environment.
• Other duties as assigned.

Skills

Venipuncture

ECG

Vital signs

Phlebotomy

Clinical judgement

Medical terminology

Teamwork

Education

High School Diploma or equivalent

EMT certification

Phlebotomy certification

CMA or CNA certification

Job description

Fortrea in Madison, WI is seeking a Clinical Research Technician II to perform clinical and administrative tasks for phase 1 studies in a fast-paced environment. You will support participants, collect vital signs, and assist with ECGs and sample handling under protocol guidance.

Open to new grads and experienced professionals; includes six weeks of paid training and a typical Mon-Fri 6:30am-2:30pm shift. This office-based role connects you with world-leading pharma and medical device sponsors.