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On-Call Clinical Research Technician/ Madison Wi (On-Site)

1-2 years
Not Disclosed
10 Oct. 7, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

On-Call Clinical Research Technician

📍 Location: Madison, WI (On-Site)
📂 Category: Clinical
🆔 Job ID: 253301
🏢 Type: On-Call, Office-Based


About the Company

As one of the world’s largest Clinical Research Organizations (CROs), we operate four Early Phase Clinical Research Units (CRUs) across the UK and US. Our mission is to advance clinical development by conducting Phase I clinical trials that establish the safety, tolerability, and pharmacokinetics of new drug candidates.

By joining us, you’ll collaborate with leading pharmaceutical, biotechnology, and medical device companies, gaining hands-on experience in early-stage clinical research. This role allows you to directly impact patient care by supporting the development of breakthrough therapies.


Role Overview

The On-Call Clinical Research Technician performs both practical and administrative activities for clinical trials in accordance with protocols, SOPs, and regulatory requirements. You’ll provide direct participant care, conduct clinical procedures, and ensure high-quality data collection in a fast-paced, electronic data environment.

This position offers the opportunity to apply your clinical knowledge, enhance technical skills, and participate in the development of new medical technologies.


Key Responsibilities

  • Perform vital sign assessments including blood pressure, pulse, weight, respiratory rate, and temperature.

  • Prepare and accurately record ECGs/Holters.

  • Collect and process biological samples as per study protocol and ensure proper distribution.

  • Monitor meals to ensure dietary compliance of study participants.

  • Assist in screening procedures and participant check-in/check-out.

  • Observe study subjects for general well-being and promptly report any concerns.

  • Prepare rooms and medical equipment for study procedures.

  • Collaborate with Study Coordinators on Failure Mode and Effects Analysis (FMEA) as required.

  • Respond to emergency situations according to clinical research standards.

  • Perform additional tasks or duties as assigned by the supervisor.


Qualifications & Requirements

🎓 Education:

  • Bachelor’s in Science preferred

  • In lieu of degree, relevant job experience will be considered

💼 Experience:

  • 1–2 years of experience as a Clinical Research Technician preferred

  • CNA / Med Tech experience advantageous

  • Clinical or non-clinical background accepted

  • Open to recent graduates with clinical exposure

🗣️ Language Skills:

  • English proficiency required (speaking, writing, and reading)

🕒 Availability:

  • Willingness to cover weekends and/or overnight shifts preferred


Work Environment

  • Fast-paced: strict adherence to study protocols; every minute counts for quality

  • 🔄 Dynamic: frequent priority shifts requiring flexibility and quick decision-making

  • 🤝 Team-Oriented: strong communication and collaboration essential

  • 💻 Technology-Based: data recorded directly in an electronic system


Why Join Us?

  • Engage directly with participants and cutting-edge medical research

  • Contribute to Phase I clinical trials that shape future patient care

  • Gain exposure to innovative drug development and regulatory practices

  • Work alongside industry leaders in a professional, mission-driven environment


🔗 Learn more: [EEO & Accommodations Request Information] (Insert official link if available)