Compliance Analyst Visa Sponsorship Jobs in Illinois
Illinois compliance analyst roles are concentrated in Chicago's financial district, insurance corridor, and healthcare networks, with major employers including JPMorgan Chase, Aon, United Airlines, and Abbott Laboratories regularly hiring for these positions. Firms in regulated industries across Chicago, Deerfield, and Schaumburg have an established track record of H-1B visa sponsorship for qualified compliance professionals.
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Department
BSD OCR - Operations Infrastructure Support
About the Department
The Office of Clinical Research (OCR) is dedicated to supporting the infrastructure for the management and administration of clinical research at The University of Chicago as well as individual research programs with the goal of improving communication, consistency, and collaboration across the Biological Sciences Division and UChicago Medicine.
To mission of the OCR is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers.
Job Summary
The job maintains regulatory compliance programs, including the interpretation of systems to identify areas of risk and may coordinate internal audits. With a moderate level of direction, participates in compliance documentation, compliance training, and compliance committee formation.
The OnCore Compliance & Monitoring Analyst supports the integrity, accuracy, and regulatory compliance of clinical research data within the Clinical Trial Management System (CTMS), OnCore.
This role is responsible for the review, monitoring, and evaluation of clinical research records to ensure completeness, consistency, and alignment with institutional policies and applicable regulatory requirements.
As a member of the Research Systems & Coverage Analysis (RSCA) Unit within the Office of Clinical Research, this position partners closely with study teams and institutional stakeholders to strengthen research data quality and operational consistency across the clinical research enterprise.
The Analyst performs routine and targeted reviews of OnCore records, identifies discrepancies across integrated research systems, and assesses adherence to required documentation and data standards.
This role provides recommendations for corrective actions, supports resolution of identified issues, supports training activities, and contributes to continuous quality improvement efforts. The position also serves as a resource for best practices in clinical research data management and OnCore utilization, helping promote standardized and compliant research operations across the institution.
Responsibilities
- Conducts routine and targeted monitoring of clinical research study records to assess compliance with institutional policies, regulatory requirements, and established research workflows.
- Performs reconciliation of clinical research data across CTMS and related institutional systems to ensure accuracy, completeness, and data integrity.
- Reviews study lifecycle documentation—including approvals, amendments, enrollment data, and protocol records, to identify discrepancies, missing information, and data quality issues.
- Evaluates adherence to institutional SOPs and processes related to study activation, maintenance, amendments, enrollment, and study closure activities.
- Documents monitoring findings and prepares formal reports summarizing observations, risk areas, trends, and recommended corrective and preventive actions (CAPAs).
- Communicates findings to principal investigators, study teams, and institutional stakeholders, providing clear guidance on remediation steps and process improvements.
- Tracks corrective and preventive actions through resolution and verifies implementation and effectiveness of remediation efforts.
- Collaborates with Research Compliance, HRPP, and other key stakeholders to support monitoring activities and promote consistent research administration practices.
- Contributes to the development and maintenance of monitoring plans, review methodologies, audit procedures, and quality assurance metrics.
- Analyzes monitoring outcomes to identify trends, recurring issues, and systemic risks, and develops summary reports to support operational improvement efforts.
- Provides education and guidance to research personnel on institutional requirements, system use, documentation standards, and best practices.
- Serves as a subject matter resource for clinical research systems compliance, data integrity, and quality assurance processes.
- Coordinates department or clinic compliance with a moderate level of guidance.
- Prepares, completes and submits all compliance documentation on a routine basis. Coordinates compliance committee meetings.
- Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
Certifications:
Preferred Qualifications
Education:
- Bachelor's degree.
Experience:
- Clinical research experience such as regulatory compliance, study coordination, quality assurance, monitoring, auditing, or related research activities.
- Experience utilizing the Clinical Trial Management System, Oncore.
- Experience conducting audits, monitoring reviews, or quality assurance assessments.
Preferred Competencies
- Proficiency with the Clinical Trial Management System, OnCore.
- Experience with electronic IRB systems.
- Knowledge of human subject research regulations and institutional research administration processes.
- Knowledge of Good Clinical Practice (GCP), FDA regulations, and applicable institutional policies.
- Proficiency with Microsoft Office applications including Word, Excel, PowerPoint, and Teams.
Working Conditions
- Office environment.
Application Documents
- Resume (required)
- Cover Letter (required)
The University of Chicago uses AI-assisted tools to streamline and augment some recruitment processes; however, AI is not used to make hiring decisions.
When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
Job Family
Legal & Regulatory Affairs
Role Impact
Individual Contributor
Scheduled Weekly Hours
40
Drug Test Required
No
Health Screen Required
No
Motor Vehicle Record Inquiry Required
No
Pay Rate Type
Salary
FLSA Status
Exempt
Pay Range
$65,000.00 - $90,000.00
The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.
Benefits Eligible
Yes
The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.
Posting Statement
The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination.
Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form.
All offers of employment are contingent upon a background check that includes a review of conviction history. A conviction does not automatically preclude University employment. Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position.
The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online at: http://securityreport.uchicago.edu. Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.
Compliance Analyst Job Roles in Illinois
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Search Compliance Analyst Jobs in IllinoisCompliance Analyst Jobs in Illinois: Frequently Asked Questions
Which companies sponsor visas for compliance analysts in Illinois?
Chicago-based financial institutions and insurance firms are among the most active sponsors for compliance analyst roles in Illinois. Companies such as JPMorgan Chase, Northern Trust, Morningstar, Aon, and Discover Financial have filed H-1B petitions for compliance positions. Healthcare organizations including Abbott Laboratories and Baxter International also sponsor compliance analysts in the suburbs north and west of Chicago.
Which visa types are most common for compliance analyst roles in Illinois?
The H-1B is the most common visa for compliance analysts in Illinois, as these roles typically require a bachelor's degree in finance, law, accounting, or a related field, meeting the specialty occupation standard. Candidates already holding L-1B status through multinational employers also transition into compliance analyst roles. TN visa eligibility may apply for Canadian or Mexican nationals in certain compliance-adjacent categories.
Which cities in Illinois have the most compliance analyst sponsorship jobs?
Chicago accounts for the large majority of compliance analyst sponsorship opportunities in Illinois, particularly in the Loop, River North, and West Loop financial and corporate districts. Suburban clusters in Deerfield, Northbrook, and Schaumburg host compliance teams for major pharmaceutical, insurance, and technology firms. Peoria and Bloomington have smaller but active compliance hiring markets tied to insurance and manufacturing companies headquartered there.
How to find compliance analyst visa sponsorship jobs in Illinois?
Migrate Mate is built specifically for international candidates and filters compliance analyst roles in Illinois by visa sponsorship status, so you're not sifting through listings from employers who won't sponsor. The platform surfaces roles from financial services, healthcare, and insurance firms in Chicago and the surrounding suburbs that have an active history of H-1B filings for compliance positions.
Are there state-specific factors that affect compliance analyst sponsorship in Illinois?
Illinois is home to the Chicago Federal Reserve district and a dense concentration of FINRA-regulated broker-dealers, which drives consistent demand for compliance analysts with finance or securities backgrounds. The state's university pipeline from University of Illinois, Northwestern, and DePaul produces graduates who often pursue compliance roles locally, making employer sponsorship infrastructure relatively well-established. Prevailing wage determinations for Illinois compliance analyst roles are set by the Department of Labor and vary by metropolitan area.
What is the prevailing wage for sponsored compliance analyst jobs in Illinois?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.