Clinical Trial Associate Visa Sponsorship Jobs in Illinois
Illinois is a strong market for clinical trial associate roles, with major employers like AbbVie, Abbott, and Baxter International headquartered in the Chicago metro area. The state's concentration of academic medical centers, contract research organizations, and pharmaceutical firms in the North Shore and Chicago suburbs creates consistent demand for CTA talent, including candidates who require visa sponsorship.
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Department BSD OCR - Post Award
About The Department
The Office of Clinical Research (OCR) is the nucleus of the clinical research enterprise, providing services, training, tools and compliance oversight to support the conduct of clinical research across the entire Biological Sciences Division and University of Chicago Medicine human subject research portfolio. The mission of the Office of Clinical Research 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. Together, we elevate the human experience with knowledge and health care.
Job Summary
The job provides professional support for pre-award and/or post-award activities relating to grant and contract proposals and funding within a department or unit. Pre-award activities include research, preparing applications, and editing proposals. Post-award activities include compliance monitoring, payment processing, and salary allocations. Performs work with moderate guidance and utilizes knowledge of University and business drivers. The Clinical Trial Financial Manager provides administrative support in an intensive customer service environment for the Clinical Trial Financial Group CTFG within the Office of Clinical Research for the Biological Sciences Division.
Responsibilities
- Serves as a primary account administrator for clinical research study accounts.
- Creates accounts and works within the financial accounting system, Oracle.
- Allocates, authorizes, monitors, and controls expenses on clinical research study accounts.
- Manages check and wire-transfer deposits and earnings invoicing for industry-funded clinical trials.
- Maintains accurate accounts receivable and payable data in OnCore CTMS and VETS (Visit Earnings Tracking System).
- Facilitates timely reconciliation and close-out of terminated clinical trial financial accounts.
- Maintains, oversees, reconciles, and corrects errors in accounts. Processes clinical research and core bills for payment.
- Partners with CT Contracts Managers on budgetary amendment implementation.
- Communicates regularly with study staff on accrual tracking and provides training in study financial management.
- Works with other administrators on the procurement process including purchasing, internal requisitioning, and personal and travel reimbursements.
- Partner with grants administrators to manage financial and administrative aspects.
- Project proposal preparation, submission, and post-award grant administration.
- Advises and assists in relationship management and communications with funding agencies, subcontractors, and others.
- Monitors expenditures on approximately 560 - 700 active individual faculty accounts.
- Proposes solutions to discovered problems and fixes according to proper policy and compares actual spending to original budget and identifies any variances with the particular attention being paid to faculty salary.
- Develops a working knowledge of University policies and procedures as well as a working knowledge of policies and procedures of various funding agencies.
- Creates and maintains excel spreadsheets and databases to track Division’s clinical research.
- Works closely with Section Administrators and Department Leadership to effectively manage faculty clinical research accounts and ensure proper spending.
- Seeks new avenues for funding and grant opportunities and ensures that notices of relevant opportunities are brought to faculty attention. Works with sponsors to draft proposal budgets in accordance with University needs, with a moderate level of guidance and direction.
- Handles straightforward post-award activities including account creations, regulatory and compliance monitoring, salary allocations, effort reporting, grant projections, cost allocations, cost center charges, equipment inventory, invoice preparation, grant closing process, and account closing.
- Prepares summaries of grants and effort allocations for Principal Investigators, meets with them and responds to their questions. Coordinates with other departments/units/divisions regarding multi investigator grants. Serves as department contact for annual audits and agency site visits.
- Performs other related work as assigned.
Education:
Minimum Qualifications
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:
- Working knowledge in Oracle, Business Objects, and academic medical operations.
- An understanding of fund accounting principles, federal and major non-federal post-award policies, allowable cost policies, and fundamental academic policies, allowable cost policies, and fundamental academic medical research accounting.
Preferred Competencies
- Strong computer skills including word processing, database management, and spreadsheet skills.
- Excellent verbal and written communication skills.
- Attention to detail.
- Flexible and adaptable.
- Knowledge of general accounting standards and auditing.
- Strong organizational skills.
- Sound financial and analytic skills.
- Research issues and propose solutions to problems.
- Demonstrated initiative in improving processes and enhancing systems.
- Exercise sound judgment, discretion and tact.
- Exceptional time management skills and the ability to handle multiple, concurrent tasks within deadlines.
- Work with individuals from across the division and University.
- Proficient in research methods and funding sources.
- Expertise with clinical trials.
- Background with federal and non-federal regulations for grant management.
- Proficiency with fund accounting.
- Familiarity with federal and non-federal grant and contract policies.
Working Conditions
- Office environment.
Application Documents
- Resume (required)
- Cover Letter (preferred)
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 Financial Management
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 $75,000.00 - $100,000.00
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.
Clinical Trial Associate Job Roles in Illinois
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Search Clinical Trial Associate Jobs in IllinoisClinical Trial Associate Jobs in Illinois: Frequently Asked Questions
Which companies sponsor visas for clinical trial associates in Illinois?
AbbVie, Abbott Laboratories, Baxter International, and Takeda Pharmaceuticals North America are among the larger Illinois-based employers with established immigration programs that have sponsored clinical trial associate roles. Contract research organizations with Illinois offices, including ICON plc and Covance, also have documented sponsorship histories. Sponsorship availability varies by position, budget cycle, and individual hiring manager, so confirming sponsorship willingness early in the application process is important.
Which visa types are most common for clinical trial associate roles in Illinois?
The H-1B visa is the most common visa for clinical trial associates in Illinois, as the role typically qualifies as a specialty occupation requiring at least a bachelor's degree in a life sciences or health-related field. Some candidates also enter through OPT or STEM OPT extensions while job searching. The TN visa applies to Canadian and Mexican nationals with qualifying degrees. L-1 visa transfers are possible for candidates relocating from a foreign affiliated office of a multinational sponsor.
Which cities in Illinois have the most clinical trial associate sponsorship jobs?
The Chicago metropolitan area accounts for the large majority of clinical trial associate sponsorship activity in Illinois. North Shore suburbs, including North Chicago, Lake Forest, and Waukegan, host AbbVie and several other pharmaceutical employers. Downtown Chicago and the medical district near the University of Illinois at Chicago and Rush University Medical Center also generate CTA openings. Rockford and Peoria have smaller but active clinical research communities tied to regional hospital networks.
How to find clinical trial associate visa sponsorship jobs in Illinois?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it easier to identify Illinois employers actively willing to sponsor clinical trial associate candidates rather than sorting through postings that exclude international applicants. Searching by role and filtering to Illinois on Migrate Mate surfaces positions at pharmaceutical companies, CROs, and academic medical centers in the Chicago metro and North Shore. Setting up alerts for clinical trial associate roles in Illinois helps catch new postings early.
What state-specific factors should clinical trial associates know about working in Illinois?
Illinois has a significant concentration of Phase I through Phase III trial activity driven by its academic medical infrastructure at institutions such as Northwestern Medicine and the University of Chicago Medicine. Employers filing H-1B petitions for clinical trial associates must meet Department of Labor prevailing wage requirements for the specific work location, which in the Chicago metro tends to reflect a competitive market rate. Illinois does not impose additional state-level licensing requirements specific to clinical trial associates beyond federal GCP training expectations.
What is the prevailing wage for sponsored clinical trial associate 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.