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.
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