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Clinical Research Lab Jobs in Wisconsin (NOW HIRING)

Lab Technician / Madison, WI (On-site)

Madison, WI · On-site

$19.25 - $25.50/hr

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Lab Technician to interact directly ...

WI · On-site

$100 - $150/hr

Drive AI model deployment and real‑world clinical integration. * Lead high‑impact ... Present research at national and international conferences. * Establish the VITAL Lab as a global ...

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Showing results 21-40

Clinical Research Lab information

See Wisconsin salary details

$49.5K

$108.3K

$190.8K

How much do clinical research lab jobs pay per year?

As of Aug 21, 2026, the average yearly pay for clinical research lab in Wisconsin is $108,340.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,800.00 and $123,600.00 per year, depending on experience, location, and employer.

What is a clinical research lab?

A clinical research lab is a specialized facility where scientific studies involving human participants are conducted to evaluate the safety and effectiveness of medications, medical devices, diagnostics, or treatment protocols. These labs play a crucial role in advancing medical knowledge by generating data that supports regulatory approvals and clinical practice guidelines. The work in such labs is highly regulated to ensure the integrity of the research and the safety of participants. Clinical research labs often collaborate with hospitals, universities, and pharmaceutical companies to conduct these studies.

What are the key skills and qualifications needed to thrive in a clinical research lab, and why are they important?

To thrive in a Clinical Research Lab, you need a solid background in biological sciences or related fields, experience with laboratory techniques, and often at least a bachelor’s degree in science. Familiarity with laboratory information management systems (LIMS), data analysis software, and regulatory compliance certifications such as Good Clinical Practice (GCP) is typically required. Strong attention to detail, effective teamwork, and clear communication skills are essential soft skills in this environment. These competencies ensure accurate data collection, regulatory adherence, and successful collaboration on research projects.

What are some common challenges faced by professionals working in a clinical research lab, and how can they be addressed?

Professionals in a clinical research lab often encounter challenges such as strict regulatory requirements, tight project timelines, and the need for meticulous attention to detail. Maintaining accurate documentation and adhering to protocols is crucial, which can be demanding under pressure. Effective communication within multidisciplinary teams—such as clinicians, data managers, and laboratory technicians—is essential for smooth workflow. Proactively seeking mentorship, staying updated on regulatory changes, and participating in team meetings can help mitigate these challenges and foster a collaborative environment.

What is the difference between Clinical Research Lab vs Clinical Research Coordinator?

AspectClinical Research LabClinical Research Coordinator
CredentialsTypically requires laboratory science degrees or certificationsRequires clinical research certifications and healthcare-related degrees
Work EnvironmentLaboratories, research facilitiesClinics, hospitals, research sites
Employer & IndustryResearch institutions, biotech companiesHospitals, clinical trial sites
Job FocusLaboratory testing, sample analysisParticipant management, study coordination

While both roles are essential in clinical research, a Clinical Research Lab focuses on laboratory testing and analysis, whereas a Clinical Research Coordinator manages participant recruitment and study logistics. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Clinical Research Lab jobs in Wisconsin?

For Clinical Research Lab jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Clinical Research Lab jobs in Wisconsin look for?

The top searched job categories for Clinical Research Lab jobs in Wisconsin are:

What cities in Wisconsin are hiring for Clinical Research Lab jobs?

Cities in Wisconsin with the most Clinical Research Lab job openings:

Infographic showing various Clinical Research Lab job openings in Wisconsin as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 16% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $108,340 per year, or $52.1 per hour.

Clinical Research Nurse (On-Call)/Madison, WI (On-Site)

Fortrea

Madison, WI • On-site

Other

Re-posted 5 days ago


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 74 rated research


Job description

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.
We are currently seeking a Clinical Research Nurse I (On-Call), to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)
This is a full-time, office/clinic-based job in Madison, WI
If you join us, you will work with some of the world's leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.
Many Nurses are drawn to this profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you'll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you'll touch many patient's lives around the world.
WHAT YOU WILL DO:
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.
Other key responsibilities:

  • Ensure that the dignity, health, safety, and welfare of participants is given the highest priority at all times
  • Be current with appropriate emergency certifications and company emergency policy and procedures
  • Respond to emergency situations based upon nursing standards
  • Utilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials
  • Utilize nursing assessment skills to observe participant general well-being and potential adverse events. Document adverse events and takes appropriate action as needed
  • Obtain Informed Consent and continue the ICF process by educating, explaining and informing participants of study procedures
  • Administer investigational compounds (inclusive of parenteral) to participants according to the protocol and applicable regulations
  • Perform study related activities such as cannulation, telemetry, holters, vital signs, ECGs, venipuncture
  • Undertake any other duties as required
Education / Experience:
  • Associates Degree or BS degree in nursing with current licensure in applicable state.
  • CPR/AED certified
  • ACLS-certified preferred upon entry to role. ACLS certification maybe be gained in role if not yet certified
  • Additional experience may be substituted for education requirements
YOU NEED TO BRING...
  • 0-1 year of related experience
  • Additional experience may be substituted for education requirements
The important thing for us is you are comfortable working in an environment that is:
  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.
Physical Requirements:
  • Ability to work in an upright and /or stationary position for 6-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

Learn more about our EEO & Accommodations request here.

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