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

Fortrea
Fortrea
0-1 years
Not Disclosed
Madison, United States
10 April 8, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Research Technician (On-Call)

Location: Madison
Job Type: Casual / On-Call
Work Model: On-Site
Job Requisition ID: 261426

Job Overview
We are seeking a dedicated Research Technician (On-Call) to support early-phase clinical research activities at our clinical research unit in Madison, Wisconsin. This role is ideal for candidates interested in clinical research, patient care, and hands-on healthcare operations. The selected candidate will work directly with healthy volunteer participants and assist in executing Phase I clinical trials, contributing to the development of innovative pharmaceutical, biotechnology, and medical device therapies.

This is an on-call position requiring availability to cover rotational day, mid, night, weekend, and holiday shifts based on business needs.

Experience Required

  • 0–1 year of related clinical, healthcare, laboratory, or research experience

  • Prior experience in clinical or patient care settings is preferred

  • Experience with phlebotomy, vital sign monitoring, or specimen collection is advantageous

Key Responsibilities

  • Perform clinical assessments including blood pressure, pulse, respiratory rate, temperature, and weight measurements

  • Conduct venipuncture and assist with blood sample collection procedures

  • Prepare and accurately record ECGs and Holter monitor readings

  • Collect, process, and distribute biological samples according to study protocols

  • Monitor participant meals to ensure dietary compliance during clinical studies

  • Assist with preparation of examination rooms and medical equipment

  • Support participant screening procedures as needed

  • Maintain a clean, safe, and organized clinical research environment

  • Ensure compliance with study protocols and timelines

  • Assist with additional research and administrative duties as assigned

Required Qualifications

  • High School Diploma or equivalent required

  • EMT, Phlebotomy, CMA, or CNA certification preferred

Preferred Skills

  • Strong clinical judgment and patient care skills

  • Ability to work accurately in a fast-paced research environment

  • Strong teamwork and interpersonal communication skills

  • Adaptability to changing priorities and schedules

  • Comfort working with electronic data capture and technology-based systems

  • High attention to detail and protocol adherence

Work Environment

  • On-site office/clinical research unit environment

  • Rotational shifts including days, mids, nights, weekends, and holidays as needed

  • Fast-paced clinical research setting with strict protocol timelines

Physical Requirements

  • Ability to stand or remain stationary for 6–8 hours per day

  • Repetitive hand and wrist movements for operating medical/lab equipment

  • Frequent bending, twisting, stooping, and crouching

  • Ability to lift and carry up to 15–20 lbs

  • Regular and reliable attendance required

Why Join This Opportunity
This role offers an excellent entry point into clinical research, Phase I trials, patient-facing healthcare, and drug development operations, providing exposure to cutting-edge therapies and clinical trial processes while working alongside leading pharmaceutical and biotechnology organizations.

Apply now to begin your career in clinical research and early-phase drug development.