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Study Monitor Jobs in Wisconsin (NOW HIRING)

Support participant screening procedures and monitor protocol-required meals. * Prepare exam rooms and ensure clinical equipment is ready for study visits. * Maintain organized, clean, and compliant ...

... studies follow established protocols, standard operating procedures, and regulatory guidelines. Responsibilities * Provide daily care for mice and rats, including feeding, watering, and monitoring ...

... studies follow established protocols, standard operating procedures, and regulatory guidelines. Responsibilities * Provide daily care for mice and rats, including feeding, watering, and monitoring ...

... monitoring. * Performs additional task list items as delegated and supervised by Charge Staff. * Reviews Study Specific Trainings and applicable protocols for a thorough understanding of the study ...

Perform study-related procedures, including: * Cannulation * Venipuncture * Vital signs collection * ECGs, telemetry, and Holter monitoring * Collect, process, and handle biological samples per ...

... monitoring, aquatic studies, stormwater compliance monitoring, and environmental permitting. Job duties will also include proposal preparation and cost estimating, and quality control reviews. The ...

... monitoring, aquatic studies, stormwater compliance monitoring, and environmental permitting. Job duties will also include proposal preparation and cost estimating, and quality control reviews. The ...

Monitors program budget (s) and approves unit expenditures * Interacts with study participants and community engaged stakeholders, conducts data collection, and monitors participants throughout study

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Showing results 1-20

Study Monitor information

See Wisconsin salary details

$15.5K

$70.6K

$126K

How much do study monitor jobs pay per year?

As of Jun 10, 2026, the average yearly pay for study monitor in Wisconsin is $70,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,177.00 and $104,097.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Study Monitor position, and why are they important?

To thrive as a Study Monitor, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as GCP), and data integrity principles, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly expected. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills. These competencies ensure high-quality study oversight, compliance with regulations, and smooth collaboration among clinical research teams.

What are some common challenges Study Monitors face during clinical trials?

Study Monitors often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing discrepancies in data, and navigating tight timelines for site visits and reporting. They must adapt quickly to evolving regulatory requirements and effectively communicate any issues or deviations to investigators and sponsors. Being proactive in identifying potential risks and fostering strong relationships with site staff can help minimize these challenges. As a result, successful Study Monitors need to be resourceful, detail-oriented, and skilled at balancing regulatory compliance with practical problem-solving in dynamic trial environments.

What is a Study Monitor job?

A Study Monitor, also known as a Clinical Research Associate (CRA), is responsible for overseeing clinical trials to ensure they comply with regulatory guidelines, study protocols, and ethical standards. They monitor site activities, review data accuracy, and ensure participant safety. Study Monitors work closely with investigators, site staff, and sponsors to ensure the integrity of trial results and adherence to Good Clinical Practice (GCP) guidelines.

What cities in Wisconsin are hiring for Study Monitor jobs? Cities in Wisconsin with the most Study Monitor job openings:
Licensed Practical Nurse

Licensed Practical Nurse

Medix

Madison, WI • On-site

$30 - $45/hr

Part-time

Medical, Dental, Vision, Retirement

Posted 2 days ago


Job description

You are applying for a position through Medix, a staffing agency. The actual posting represents a position at one of our clients.
Job Summary
Our client is seeking a Licensed Practical Nurse to support clinical research staff in conducting study visits and collecting participant data while ensuring strict adherence to study protocols and timelines.
Key Responsibilities
  • Obtain and document vital signs (BP, pulse, temperature, respirations, weight).
  • Perform venipuncture and assist with collection and processing of biological samples per protocol.
  • Prepare and record ECGs and assist with Holter monitor setup.
  • Support participant screening procedures and monitor protocol-required meals.
  • Prepare exam rooms and ensure clinical equipment is ready for study visits.
  • Maintain organized, clean, and compliant clinical workspaces.
  • Accurately enter study data into electronic systems and assist with general study operations.

Qualifications
  • High School Diploma or equivalent required.
  • 0-1 year of healthcare or clinical experience preferred.
  • EMT, Phlebotomy, CMA, CNA, or Paramedic certification preferred (Paramedics must hold state certification).

Benefits
  • Paid Sick Leave (Medix provides paid sick leave according to state and local sick leave ordinances).
  • Health Benefits / Dental / Vision (Medix offers 6 different health plans: 3 Major Medical Plans, 2 Fixed Indemnity Plans (Standard and Preferred), and 1 Minimum Essential Coverage (MEC) Plan. Eligibility for health benefits is based on verifying that an average of 30 hours per week during the first 4 weeks of the work assignment has been met. If you meet eligibility requirements and take action to enroll, you will be covered no earlier than 60 days into your assignment, depending on plan selection(s)).
  • 401k (Eligible on the first 401k open enrollment date following 6 consecutive months on assignment. 401k Open Enrollment dates are 1/1, 4/1, 7/1, and 10/1).
  • Short Term Disability Insurance.
  • Term Life Insurance Plan.

* We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).
Medix Overview:
With over 20 years of experience connecting organizations with highly qualified professionals, Medix is a leading provider of workforce solutions for clients and candidates across the healthcare, scientific, technology, and government industries. Through our core purpose of positively impacting lives, we're dedicated to creating opportunities for job seekers at some of the nation's top companies. As an award-winning career partner, Medix is committed to helping talent find fulfilling and meaningful work because our mission is to help you achieve yours.
* As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.

Medix Staffing Solutions logo

About Medix Staffing Solutions

Sourced by ZipRecruiter

Since 2001, we’ve been dedicated to helping you achieve your goals. Medix was created to become a leading provider of workforce solutions for clients and candidates across the healthcare and life sciences industries. Today, we are that leader. Headquartered in Chicago, we have 23 offices across the United States, and staff talent around the world. Medix is committed to fulfilling our core purpose as an organization: to positively impact the lives of our talent, clients, and teammates through employment, philanthropy, and opportunity. The combination of purpose and values has nurtured our thriving culture that encourages our internal team to excel at work and in everyday life.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Chicago, IL, US