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Clinical Site Monitor Jobs in Illinois (NOW HIRING)

AbbVie

Site Management Lead

North Chicago, IL · On-site

The SML provides direction and operational expertise for all Clinical Site Management (CSM ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

The SML provides direction and operational expertise for all Clinical Site Management (CSM ... Experience in industry clinical research including monitoring or project management or equivalent ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

The SML provides direction and operational expertise for all Clinical Site Management (CSM ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

If assigned to area site execution activities, responsible and accountable for directing site ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

The SML provides direction and operational expertise for all Clinical Site Management (CSM ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

If assigned to area site execution activities, responsible and accountable for directing site ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL

If assigned to area site execution activities, responsible and accountable for directing site ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

The SML provides direction and operational expertise for all Clinical Site Management (CSM ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

If assigned to area site execution activities, responsible and accountable for directing site ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

If assigned to area site execution activities, responsible and accountable for directing site ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

AbbVie

Site Management Lead

North Chicago, IL · On-site

$109.50K/yr

If assigned to area site execution activities, responsible and accountable for directing site ... A minimum of 5 years + of industry clinical research experience including 2 year of monitoring or ...

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Clinical Site Monitor information

See Illinois salary details

$11

$19

$27

How much do clinical site monitor jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical site monitor in Illinois is $19.60, according to ZipRecruiter salary data. Most workers in this role earn between $16.06 and $22.60 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Site Monitor, and why are they important?

To thrive as a Clinical Site Monitor, you need a background in life sciences or healthcare, solid knowledge of clinical trial protocols, and experience with regulatory guidelines such as GCP. Familiarity with electronic data capture (EDC) systems, trial master files (TMF), and certifications like ACRP or SOCRA are typically valued. Strong attention to detail, organizational abilities, and effective communication skills help you excel in monitoring sites and collaborating with site staff. These competencies ensure clinical trial integrity, regulatory compliance, and the reliable collection of high-quality data.

What are the main challenges Clinical Site Monitors face when ensuring site compliance during clinical trials?

Clinical Site Monitors often encounter challenges such as maintaining consistent communication with site staff, ensuring timely and accurate data entry, and addressing protocol deviations. They must carefully balance multiple sites and timelines, handle regulatory documentation, and quickly resolve issues that could impact trial integrity. Working proactively with cross-functional teams and fostering strong relationships with site personnel are key to overcoming these challenges and ensuring successful trial outcomes.

What is a Clinical Site Monitor?

A Clinical Site Monitor, also known as a Clinical Research Associate (CRA), is a professional responsible for overseeing clinical trials at research sites. Their main duties include ensuring that trials are conducted in compliance with regulatory requirements, protocols, and good clinical practice (GCP) guidelines. They visit clinical sites to monitor data integrity, patient safety, and adherence to study procedures. Clinical Site Monitors act as the primary link between the study sponsor and the site staff, helping resolve issues and ensuring accurate data collection throughout the trial.

What job makes $10,000 a month without a degree?

A Clinical Site Monitor typically earns between $5,000 and $12,000 per month depending on experience and location, with some senior or specialized roles reaching or exceeding $10,000. These positions require knowledge of clinical trial protocols, strong organizational skills, and often certification, but they do not always require a college degree. High earnings are often associated with freelance or contract work in the clinical research industry.

What is the difference between Clinical Site Monitor vs Clinical Research Associate?

AspectClinical Site MonitorClinical Research Associate
CertificationsTypically requires GCP training, RAC, or similar certificationsOften holds GCP certification, CRA certification, or equivalent
Work EnvironmentOn-site at clinical trial sites, monitoring progress and complianceCan be on-site or remote, overseeing multiple sites or studies
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, academic institutions

Both roles focus on ensuring clinical trial compliance and data integrity. The Clinical Site Monitor primarily works on-site at trial locations, while the Clinical Research Associate may have a broader role, including remote monitoring. Both positions require similar certifications and are integral to clinical research operations.

What are popular job titles related to Clinical Site Monitor jobs in Illinois? For Clinical Site Monitor jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Clinical Site Monitor jobs in Illinois look for? The top searched job categories for Clinical Site Monitor jobs in Illinois are:
Clinical Site Monitor jobs near you
Infographic showing various Clinical Site Monitor job openings in Illinois as of May 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $40,776 per year, or $19.6 per hour.
PS Clinical Site Monitor

PS Clinical Site Monitor

University of Utah

Campus, IL • Hybrid

Full-time

Medical, Retirement

Posted 23 days ago

University Of Utah rating

7.2

Company rating: 7.2 out of 10

Based on 157 frontline employees who took The Breakroom Quiz

327th of 528 rated colleges and universities

Job description

Details
Open Date 05/05/2026 Requisition Number PRN44938B Job Title PS Clinical Site Monitor Working Title Clinical Site Monitor Career Progression Track F Track Level FLSA Code Administrative Patient Sensitive Job Code? Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP Area President Department 01345 - HCI Clinical Resrch Compliance Location Campus City Salt Lake City, UT Type of Recruitment External Posting Pay Rate Range 47600 to 75000 Close Date 08/15/2026 Priority Review Date (Note - Posting may close at any time) Job Summary
The Clinical Site Auditor reviews HCI Investigator Initiated Trials (IITs) for accuracy, internal consistency, and compliance with applicable regulations, standard operating procedures (SOP) and GCP guidelines. The auditor is a member of the Research Compliance Office and conducts audits on oncology/hematology clinical trials with varying complexity and risk levels including phase I, first in man trials.
Audits of HCI IITs are performed independent of routine study monitoring and in general, are conducted to verify the effectiveness of routine monitoring. The Auditor will verify during each audit overall compliance to the study protocol including review of subject eligibility, informed consent, disease outcome, AEs and toxicity reporting. The Auditor will also ensure regulatory documentation and completeness of essential documents, investigational drug/pharmacy records, and data quality by auditing the electronic Case Report Forms. The Auditor reviews previous audit reports and monitoring letters to verify correction of issues/findings or to discover any recurring issues or negative trends that may exist. Additionally, the Auditor will work with the study teams to develop Corrective and Preventive Action Plans (CAPAs) when needed and ensure any findings are brought to resolution. Study subject records or research charts are audited to ensure the authenticity of study conduct and validity of study results and to ensure inspection readiness by regulatory authorities.
This position will work with external sites participating in our IITs by auditing all sites on a routine basis, obtaining access to their electronic platforms and working with external sites to ensure their internal processes are being done per SOP and study contracts. Audits are performed remotely, however travel to the sites may be required.
This job has the ability to be a hybrid schedule of remote and in office work.
Huntsman Cancer Institute is committed to cancer prevention, care, and survivorship for all communities within the area we serve - which includes Idaho, Montana, Nevada, Utah, and Wyoming - with impact worldwide.

In your cover letter or during your interview process, we invite you to share how your professional experiences have prepared you to serve as a member of our team as we work to reduce the cancer burden experienced by all people and communities. This may include description of your prior experiences related to research, prevention, clinical care, community engagement/outreach, training, administration, or other areas relevant to Huntsman Cancer Institute's mission and this position.
Responsibilities
Essential Functions
  1. Oversee, coordinate and conduct routine audits on cancer related investigator-initiated clinical trials at Huntsman Cancer Institute, as well as other external participating cancer centers, in accordance with the National Cancer Institute approved Data and Safety Monitoring Plan to ensure compliance with study protocol, University, state and federal guidelines.
  2. Compile comprehensive reports for Principal Investigators, the Data and Safety Monitoring Committee (DSMC) and other committees as assigned.
  3. Analyze and document audit process, results, and outcome. Report outcomes to the DSMC.
  4. Determine the validity of collected data, conduct periodic data audits, assessing process shortfalls, and developing effective safeguards to reduce risk in clinical research.
  5. Recommend corrections to audit findings, assist teams in the development of CAPAs and other enhancements to operating policies and procedures as well as study protocols. Develop departmental SOPs.
  6. Serve as the primary contact and expert regarding regulatory agency standards governing clinical trials.
  7. Conduct quality assurance reviews on non-IIT cancer related clinical trials to ensure compliance with study protocol, university, state, and federal guidelines.
  8. Develop, coordinate and participate in educational and training programs to enhance compliance and awareness of compliance issues.
  9. Work with PI and study team to ensure compliance with the protocol, GCPs, applicable regulations and SOPs in order to protect the rights, safety and well-being of research participants and to protect the integrity of study data.
  10. Maintain current knowledge regarding federal and state guidance, including Good Clinical Practice (GCP).
  11. Conduct routine audits at HCI and external participating sites and work with the sites to ensure study compliance.
  12. Project manage assigned clinical trials by facilitating study team questions, study registrations, training on the protocol and acting as a liaison to the Data and Safety Monitoring Committee.
  13. Provide project management support for low risk investigator-initiated trials including patient registrations.
This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job
Minimum Qualifications
Bachelor's degree in a health science or related field or equivalency (one year of education can be substituted for two years of related work experience); and four years of clinical research experience that includes regulatory compliance monitoring/auditing, IRB application submission, and experience in human subjects research. Must have a working knowledge of FDA, ICH, and other regulatory compliance; an understanding of medical terminology and technical writing experience. Excellent interpersonal communication (including oral and written) and leadership skills also required. Must be proficient in Microsoft Office and possess the ability to learn new software programs.
This position is patient-sensitive and must fulfill all associated requirements. We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.
Preferences include credentialing as a Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), and/or Certified Clinical Research Professional (CCRP). Prior experience as an industry CRA or Monitor is also preferred.
Hiring department may require certification by an appropriate certifying body within two years of hire.
Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.
Preferences
  • Prior experience working in cancer related research. Knowledge of oncology/hematology with strong understanding of medical terminology.
  • An understanding of University operations, policies and technology is preferred.
Type Benefited Staff Special Instructions Summary Additional Information
The University is a participating employer with Utah Retirement Systems ("URS"). Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work). Contact Human Resources at (801) 581-7447 for information. Individuals who previously retired and are receiving monthly retirement benefits from URS are subject to URS' post-retirement rules and restrictions. Please contact Utah Retirement Systems at (801) 366-7770 or (800) 695-4877 or University Human Resource Management at (801) 581-7447 if you have questions regarding the post-retirement rules.
This position may require the successful completion of a criminal background check and/or drug screen.
The University of Utah values candidates who have experience working in settings with students and possess a strong commitment to improving access to higher education.
Veterans' preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities.
Consistent with state and federal law, the University of Utah does not discriminate based upon race, ethnicity, color, religion, national origin, age, disability, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, pregnancy-related conditions, genetic information, or protected veteran's status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education programs or activities extends to admission and employment. Inquiries about the application of Title IX and its regulations may be referred to the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both.
To request a reasonable accommodation for a disability or if you or someone you know has experienced discrimination or sexual misconduct including sexual harassment, you may contact the Director/Title IX Coordinator in the Office of Equal Opportunity and Title IX (OEO). More information, including the Director/Title IX Coordinator's office address, electronic mail address, and telephone number can be located at the: University of Utah NonDiscrimination page.
Online reports may be submitted at https://oeo.utah.edu

https://publicsafety.utah.edu/safetyreport/ This report includes statistics about criminal offenses, hate crimes, arrests and referrals for disciplinary action, and Violence Against Women Act offenses. They also provide information about safety and security-related services offered by the University of Utah. A paper copy can be obtained by request at the Department of Public Safety located at 1658 East 500 South.
As per University of Utah policy 5-108: Transfer of Benefits Eligible Staff Members, a new hire to the University of Utah who is still serving a 12 month probationary period will not be hired into another University of Utah job (a transfer) until the successful completion of the probationary period.

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About University of Utah

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The University of Utah is the state’s flagship institution of higher education, with 18 schools and colleges, more than 100 undergraduate majors and graduate programs, and an enrollment of more than 38,000 students. It is a member of the Association of American Universities—an invitation-only, prestigious group of 71 leading research institutions. The U is advancing a new national model for higher education that delivers societal impact through education, research, health care, and community service, while making social, economic, and cultural contributions that improve lives across Utah and around the world.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Salt Lake City, UT, US

Year founded

1850

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