E-3 Visa Clinical Trial Manager Jobs
Clinical Trial Manager roles qualify as E-3 specialty occupations, requiring a bachelor's degree in life sciences, nursing, or a related clinical field. Australian professionals can secure E-3 visa sponsorship without competing in the H-1B lottery, and the visa renews indefinitely as long as your sponsoring employer remains active.
Find E-3 Visa Clinical Trial Manager JobsOverview
Showing 5 of 11+ Clinical Trial Manager jobs










See all Clinical Trial Manager Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Trial Manager roles.
Get Access To All Jobs
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:
-
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.
-
Support clinical trial financial operations through data entry, record maintenance, payment processing, and financial tracking across multiple research administration and financial management systems.
-
Assist with the preparation, maintenance, and reporting of financial, study, and enrollment metrics to support operational monitoring, decision-making, and compliance requirements.
-
Perform data validation, quality assurance reviews, and data cleanup activities to ensure accuracy, completeness, and integrity of research and financial data.
-
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.
-
Monitor and respond to sponsor, investigator, and internal stakeholder inquiries regarding study status, budgets, contracts, and financial operations.
-
Manage the OCCT Budget & Contract Management inbox, triaging requests, coordinating responses, and ensuring timely resolution of issues and inquiries.
-
Maintain accurate documentation for study budgets, funding proposals, contracts, financial records, standard operating procedures (SOPs), and other research administration processes.
-
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.
-
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:
-
Bachelor’s Degree or three+ years of relevant experience
-
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.
-
Ability to interpret cost language present in the CTA and budget required. Ability to interpret research protocol information essential.
-
Strong understanding of research billing compliance preferred.
-
One to two years of work experience in healthcare finance (patient billing, collections, account reconciliations, etc) preferred.
-
Working knowledge of medical terminology preferred.
-
Ability to work independently and as a member of a team and follow through on assignments with minimal direction required.
-
Demonstrated accuracy and precision, attention to detail, and exceptional organizational skills essential.
-
Strong verbal and written communication skills required.
-
Ability to manage large quantities of data in a manner which facilitates sharing of information
-
Ability to handle high volume of work with changing priorities and constant interruptions and establish priorities and deadlines required.
-
Ability to prepare accurate documentation of events required. Ability to maintain confidential material and information required.
-
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
See all E-3 Visa Clinical Trial Manager Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new E-3 Visa Clinical Trial Manager Jobs.
Get Access To All JobsTips for Finding E-3 Visa Sponsorship as a Clinical Trial Manager
Translate your AHPRA credentials for U.S. employers
Australian clinical trial certifications and AHPRA registration don't map directly to U.S. standards. Frame your credentials in terms of ICH-GCP compliance, FDA-regulated trial experience, and any ACRP or SOCRA certifications to signal immediate readiness to U.S. hiring managers.
Target CROs with established Australian hiring pipelines
Contract research organizations like ICON, Labcorp Drug Development, and IQVIA regularly sponsor E-3 visas because they already operate in Australia and understand the visa. Prioritize these employers early, their HR teams won't need educating on the E-3 process.
Search for verified E-3 sponsorship roles on Migrate Mate
Use Migrate Mate to filter Clinical Trial Manager roles by employers with active E-3 and LCA filing history. This cuts out roles where sponsorship is listed as possible but never actioned, saving weeks of back-and-forth with recruiters.
Clarify sponsor eligibility before the offer stage
Some sponsors are biotech startups without an established DOL wage compliance process. Ask early whether the employer has filed an LCA before, if not, confirm they're prepared to engage legal counsel or use Migrate Mate's E-3 filing service to handle your LCA and visa paperwork before you give notice at your current job.
Confirm the role meets DOL specialty occupation standards
A Clinical Trial Manager title doesn't automatically satisfy the E-3 specialty occupation requirement. The job description must specify a degree requirement in a relevant field, not just preferred qualifications, or your LCA and visa application faces rejection at the DOL certification stage.
Request E-3 processing at an Australian consulate, not by mail
Applying for the E-3 visa stamp at a U.S. consulate in Sydney or Melbourne is faster than USCIS change-of-status processing from within the U.S. If you're currently onshore, factor the consulate appointment wait time into your employer's proposed start date.
E-3 Visa Clinical Trial Manager: Frequently Asked Questions
How do I find Clinical Trial Manager jobs with E-3 visa sponsorship?
Migrate Mate is the most direct way to search, it filters Clinical Trial Manager roles by employers with confirmed E-3 and LCA filing history, so you're not applying blindly to positions where sponsorship is listed as possible but rarely actioned. CROs and large pharma employers are the most consistent E-3 sponsors in clinical research.
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 the E-3 visa work better than the H-1B for Clinical Trial Managers?
For Australian nationals, the E-3 is significantly more practical. There's no annual lottery, no cap that fills within days, and no random selection risk. You can apply directly at a U.S. consulate in Australia once you have a certified LCA and job offer, with the visa typically processed within weeks rather than months.
What qualifications does a Clinical Trial Manager need to qualify for an E-3?
You need a bachelor's degree or higher in a relevant field, life sciences, nursing, pharmacy, or biomedical science are the most commonly accepted. The job offer itself must also specify a degree requirement, not just a preference. Australian three-year bachelor's degrees are generally accepted as equivalent to a U.S. four-year degree for E-3 purposes.
Can a biotech startup sponsor my E-3 visa as a Clinical Trial Manager?
Yes, any U.S. employer can sponsor an E-3, including early-stage biotechs. The requirement is that they file a certified LCA with the DOL before your visa application. Smaller companies without prior sponsorship experience often need support navigating the DOL wage compliance and LCA filing process, so confirm their readiness before accepting an offer.