Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Research Technician Iii

Fortrea
Fortrea
2-3 years
Not Disclosed
Madison, United States
10 Feb. 14, 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

Job Title: Research Technician III – Early Phase Clinical Trials | Madison, Wisconsin (On-Site)

Location: Madison, Wisconsin, United States
Job Category: Clinical Research / Clinical Operations
Employment Type: Full-Time (On-Site Clinic-Based Role)
Experience Required: Bachelor’s degree in a related field with clinical research experience preferred; prior Research Technician I experience may substitute for degree requirement

About the Organization

Join Fortrea, one of the world’s leading Contract Research Organizations (CROs), operating Early Phase Clinical Research Units across the United States and United Kingdom. Fortrea partners with global pharmaceutical, biotechnology, and medical device companies to advance therapies through Phase I clinical trials, focusing on safety, tolerability, and pharmacokinetics.

Position Overview

Fortrea is seeking a Research Technician III to support Early Phase clinical trials at its Madison, Wisconsin unit. This advanced-level clinical research technician role combines direct participant interaction with training coordination responsibilities within Clinical Operations.

You will work with healthy volunteer participants across diverse study types, including first-in-human trials, ascending dose studies, food effect studies, and drug-to-drug interaction protocols. This role is ideal for experienced clinical research professionals who thrive in structured, protocol-driven environments and are ready to take on training leadership responsibilities.

Key Responsibilities

Clinical Research Operations

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

  • Prepare and accurately record ECGs and Holter monitor readings

  • Collect, process, and distribute biological samples per protocol requirements

  • Monitor participant dietary compliance during study confinement

  • Assist with screening procedures and study-related clinical tasks

  • Perform IV cannulation when required

  • Assist with quality control (QC) of source documentation and Case Report Forms (CRFs)

  • Transcribe and verify data from source documentation into CRFs for simple to complex studies

  • Maintain accurate and timely electronic research documentation

  • Ensure participant safety, dignity, and confidentiality at all times

  • Handle participant concerns and inquiries professionally

  • Support check-in and check-out processes for study participants

  • Collaborate with Study Coordinators on risk mitigation planning (FMEA)

Training and Development Leadership

  • Assist with planning and coordinating Clinical Operations training programs

  • Develop and maintain training materials and documentation

  • Conduct onboarding and training sessions for new hires, including:

    • Clinical research fundamentals

    • Regulatory compliance topics

    • Clinical and laboratory skills

    • Bedside electronic data capture systems

  • Conduct “Train the Trainer” sessions as required

  • Track onboarding progress and provide weekly updates to supervisors

  • Identify and escalate potential performance or training delays

  • Coordinate training schedules and practical learning opportunities

  • Support ongoing training initiatives for existing staff

Required Qualifications

  • Bachelor of Science (BS) degree in a related life sciences or healthcare field

  • Basic Life Support (BLS) certification required

  • Prior Research Technician I experience may substitute for degree requirement

  • Working knowledge of regulatory requirements and ICH-GCP principles

  • Strong understanding of clinical research documentation and quality control processes

Preferred Experience

  • Experience in Early Phase (Phase I) clinical trials

  • Prior experience training or mentoring clinical staff

  • Proficiency in electronic data capture (EDC) systems

  • Experience performing IV cannulation

Work Environment Expectations

  • Fast-paced, compliance-driven clinical research environment

  • Strict adherence to study protocols and regulatory standards

  • Frequent priority changes requiring adaptability

  • Strong emphasis on teamwork and communication

  • Technology-enabled data collection systems

Compensation and Benefits

Employees working 20 or more hours per week are eligible for comprehensive benefits, including:

  • Medical, Dental, and Vision Insurance

  • Life Insurance and Short-Term/Long-Term Disability coverage

  • 401(k) Retirement Plan

  • Paid Time Off (PTO)

  • Employee Recognition Programs

  • Employee Resource Groups (ERGs)

Physical Requirements

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

  • Repetitive hand and wrist movements for operating clinical and laboratory equipment

  • Frequent bending, twisting, and occasional stooping

  • Ability to lift and carry 15–20 lbs

  • Reliable attendance with flexibility for varied hours as required

Why Join Fortrea

As a Research Technician III in Madison, you will contribute to the safe execution of early-phase clinical trials while playing a key role in training and developing future clinical operations staff. This position offers hands-on exposure to cutting-edge investigational therapies and a pathway to advanced clinical research leadership roles.

Apply now through ThePharmaDaily.com to advance your career in early-phase clinical research and clinical operations leadership.