E-3 Visa Clinical Trial Associate Jobs
Clinical Trial Associate roles in the U.S. qualify for E-3 visa sponsorship when the position requires a bachelor's degree in a life sciences, health sciences, or related field. The E-3 has no lottery and no annual cap, making it a reliable path for Australian professionals with a sponsor and a qualifying offer.
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INTRODUCTION
Ann & Robert H. Lurie Children’s Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider in the region with a 140-year legacy of excellence, kids and their families are at the center of all we do. Ann & Robert H. Lurie Children’s Hospital of Chicago is ranked in all 10 specialties by the U.S. News & World Report.
LOCATION
Simpson Querrey Biomedical Research Center
JOB DESCRIPTION
The Clinical Trial Financial Specialist is an integral member of the Office of Clinical and Community Trials (OCCT), playing an essential role in supporting the financial and administrative management of clinical research studies.
This position is responsible for financial tracking, payment processing, budget and contract support, data management, and reporting activities that support both the Financial Management and Budget and Contract Management teams within the Clinical Research Finance (CRF) service line. Reporting to the Associate Director, CRF, the Clinical Trial Financial Specialist ensures the accurate entry and maintenance of financial and study related data across multiple research administration systems. The role contributes to the development and management of study budgets, maintains compliant financial records, processes research-related transactions, and prepares reports to support operational and financial decision-making. Through attention to detail, collaboration, and a commitment to accuracy, this position helps ensure adherence to institutional policies, sponsor requirements, and regulatory standards while supporting the successful execution of clinical trials.
Essential Job Functions:
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Manage the Financial Management payment inbox which includes tracking the receipt, reconciliation, and application of clinical trial payments, including EFT, check, and lockbox remittances, ensuring accurate financial tracking and timely resolution of unapplied payments.
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Support clinical trial financial operations through data entry, record maintenance, payment processing, and financial tracking across multiple research administration and financial management systems.
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Assist with the preparation, maintenance, and reporting of financial, study, and enrollment metrics to support operational monitoring, decision-making, and compliance requirements.
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Perform data validation, quality assurance reviews, and data cleanup activities to ensure accuracy, completeness, and integrity of research and financial data.
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Support the development, submission, activation, and maintenance of funding proposals, awards, and study records within research administration systems, including Huron/RASCAL and other institutional platforms.
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Monitor and respond to sponsor, investigator, and internal stakeholder inquiries regarding study status, budgets, contracts, and financial operations.
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Manage the OCCT Budget & Contract Management inbox, triaging requests, coordinating responses, and ensuring timely resolution of issues and inquiries.
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Maintain accurate documentation for study budgets, funding proposals, contracts, financial records, standard operating procedures (SOPs), and other research administration processes.
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Collaborate closely with all members of Research Operations and Conduct, Clinical Research Services, Clinical Research Finance, and other stakeholders to facilitate efficient study startup, financial setup, contract execution, and ongoing study management.
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Contribute to process improvement initiatives by identifying discrepancies, recommending corrective actions, enhancing data quality, and supporting other clinical trial financial and administrative functions as assigned.
KNOWLEDGE, SKILLS AND ABILITIES:
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Bachelor’s Degree or three+ years of relevant experience
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One to two years experience in clinical research conduct, clinical research regulatory compliance, clinical research billing, and/or clinical research/trial budget and contract management preferred. Understanding of coverage analysis, study budgets, informed consent forms, and CTA cost language preferred.
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Ability to interpret cost language present in the CTA and budget required. Ability to interpret research protocol information essential.
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Strong understanding of research billing compliance preferred.
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One to two years of work experience in healthcare finance (patient billing, collections, account reconciliations, etc) preferred.
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Working knowledge of medical terminology preferred.
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Ability to work independently and as a member of a team and follow through on assignments with minimal direction required.
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Demonstrated accuracy and precision, attention to detail, and exceptional organizational skills essential.
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Strong verbal and written communication skills required.
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Ability to manage large quantities of data in a manner which facilitates sharing of information
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Ability to handle high volume of work with changing priorities and constant interruptions and establish priorities and deadlines required.
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Ability to prepare accurate documentation of events required. Ability to maintain confidential material and information required.
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Personal computer skills; functional experience with integrated software systems and proficient in Microsoft Office applications.
Education
PAY RANGE
$54,600.00-$89,273.60 Salary
At Lurie Children’s, we are committed to competitive and fair compensation aligned with market rates and internal equity, reflecting individual contributions, experience, and expertise. The pay range for this job indicates minimum and maximum targets for the position. Ranges are regularly reviewed to stay aligned with market conditions. In addition to base salary, Lurie Children’s offer a comprehensive rewards package that may include differentials for some hourly employees, leadership incentives for select roles, health and retirement benefits, and wellbeing programs. For more details on other compensation, consult your recruiter or click the following link to learn more about our benefits.
BENEFIT STATEMENT
For full time and part time employees who work 20 or more hours per week we offer a generous benefits package that includes:
- Medical, dental and vision insurance
- Employer paid group term life and disability
- Employer contribution toward Health Savings Account
- Flexible Spending Accounts
- Paid Time Off (PTO), Paid Holidays and Paid Parental Leave
- 403(b) with a 5% employer match
Various voluntary benefits:
- Supplemental Life, AD and Disability
- Critical Illness, Accident and Hospital Indemnity coverage
- Tuition assistance
- Student loan servicing and support
- Adoption benefits
- Backup Childcare and Eldercare
- Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
- Discount on services at Lurie Children’s facilities
- Discount purchasing program
DIVERSITY AND INCLUSION STATEMENT
At Ann & Robert H. Lurie Children’s Hospital of Chicago and its affiliates (collectively “Lurie Children’s”), we embrace and celebrate diversity and equity in a serious way. We are committed to building a team with a variety of backgrounds, skills, and viewpoints — recognizing that diverse identities strengthen our workplace and the care we can provide to the Chicago community and beyond. We treat everyone fairly, appreciate differences, and make meaningful connections that foster belonging and allyship. This is a place where you can be your best, so we can give our best to the patients and families who trust us with their care.
Lurie Children’s and its affiliates are equal employment opportunity employers. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law.
For questions about how to request an accommodation please contact: employeehealth@luriechildrens.org
AI NOTICE
Lurie Children’s utilizes certain AI-enabled features within our recruiting platform to support candidate engagement and assist recruiters in identifying and prioritizing applicants whose experience aligns with job requirements. All employment decisions are made by individuals.
It is a civil rights violation with respect to recruitment, hiring, promotion, or employment for an employer to use artificial intelligence that has the effect of subjecting employees to discrimination on the basis of protected classes under the Illinois Human Rights Act or to use zip codes as a proxy for protected classes.
For questions about the use of artificial intelligence in this process or any additional support, please contact: peoplequestions@luriechildrens.org
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Get Access To All JobsTips for Finding E-3 Visa Sponsorship as a Clinical Trial Associate
Translate your Australian credentials for U.S. employers
CTA roles in the U.S. typically require ICH-GCP certification and familiarity with FDA regulatory frameworks. Map your TGA or sponsor experience to FDA equivalents before interviews so hiring managers can immediately see the overlap.
Target sponsors with active FDA IND portfolios
Pharmaceutical companies, CROs, and academic medical centers running active Investigational New Drug trials are your strongest E-3 visa targets. Their regulatory affairs teams already understand visa sponsorship and expect to file LCAs for clinical staff.
Get your LCA filed before accepting a start date
Your employer must have a certified Labor Condition Application from DOL before you can schedule your consulate appointment. Build at least two to three weeks for DOL processing into your negotiated start date so neither side faces a gap.
Clarify the specialty occupation standard with your hiring manager
Some CTA postings list a degree as preferred rather than required. That wording can disqualify the role under USCIS specialty occupation rules. Confirm the job description explicitly states a bachelor's degree is required before the offer is finalized.
Use Migrate Mate's E-3 filing service for your LCA and visa paperwork
Once you have a written offer, Migrate Mate's E-3 filing service manages the LCA submission, DS-160, and consulate prep end-to-end. This removes the administrative burden from smaller sponsors who haven't filed E-3s before.
Prepare a protocol-specific work history summary for your consulate interview
Consular officers assess whether your qualifications match the offered CTA role. A one-page summary linking your degree and trial experience to the specific therapeutic area and protocol type in the job description strengthens your nonimmigrant intent case.
E-3 Visa Clinical Trial Associate: Frequently Asked Questions
How do I find Clinical Trial Associate jobs with E-3 visa sponsorship?
Migrate Mate filters job listings specifically for E-3 visa sponsorship, so you can search Clinical Trial Associate roles without sorting through employers who only hire U.S. citizens or permanent residents. Focusing on CROs, large pharmaceutical companies, and academic medical centers with active clinical trial programs gives you the strongest pool of willing E-3 sponsors.
How much does it cost to get an E-3 visa?
Migrate Mate's E-3 filing service covers the entire process for $499, including the Labor Condition Application, visa document preparation, and consulate appointment guidance. Traditional immigration lawyers charge $2,000–$5,000+ for the same work. The E-3 has less paperwork than most work visas, so paying thousands for legal help is usually unnecessary.
Does a Clinical Trial Associate role qualify as a specialty occupation for the E-3?
Yes, provided the job description requires a bachelor's degree or higher in a specific field such as life sciences, nursing, or health sciences. Generic postings that accept any degree or list education as preferred rather than required can fail the USCIS specialty occupation test, so the offer letter and job description must reflect a degree requirement tied to the role.
How does the E-3 compare to the H-1B for Clinical Trial Associate roles?
The E-3 has no lottery, no annual cap, and can be applied for at any time of year, unlike the H-1B visa which requires registration in April and selection by random draw. For Australian CTA professionals, this means a confirmed job offer translates directly into a visa application rather than a lottery gamble. Renewals are also indefinite as long as you maintain qualifying employment.
Can I transfer my E-3 status if I move between clinical trial sponsors in the U.S.?
Yes, but each employer change requires a new LCA certified by DOL and a new visa application or change of status filing. Unlike H-1B portability rules, the E-3 does not allow you to start work with a new sponsor while a petition is pending. You need the new LCA certified and, if applying abroad, a new visa stamp before starting your next role.