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Contractual Irb Analyst Jobs (NOW HIRING)

Clinical Contracts Analyst (REMOTE)

Minneapolis, MN · On-site +1

$72K - $87K/yr

... IRB oversight, and other reimbursable costs for clinical trials. • Manage contractual and ... analytics, reporting, and business intelligence support for clinical trials. • Track timelines ...

Clinical Contracts Analyst (REMOTE)

Minneapolis, MN · Remote

$72K - $87K/yr

... fees, IRB oversight, and other reimbursable costs for clinical trials. Manage contractual and ... Provide data management, analytics, reporting, and business intelligence support for clinical ...

Ability to understand contractual issues, relevant contract law and health care policy within ... Board (IRB), and Institutional Animal Care and Use Committee approvals (IACUC). * Ensures ...

... analyses, coverage analyses, and research billing grids. * Collaborates with investigators ... IRB, finance offices, and institutional service providers to ensure alignment across contractual ...

... contractual timelines and expectations. * Partner with fiscal staff to manage reimbursement ... data analysis, regulatory compliance, and IRB processes. * Demonstrated ability to work ...

Project Manager

Syracuse, NY · On-site

$66K - $70K/yr

... contractual requisites; and external market analyses. Staff Level S5 FLSA Status Exempt Hours ... IRB review, study design, analysis, and research-related software programs (reference management ...

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Contractual Irb Analyst information

What are the key skills and qualifications needed to thrive as a Contractual IRB Analyst, and why are they important?

To thrive as a Contractual IRB Analyst, you need a solid understanding of human subjects research regulations, experience with protocol review, and at least a bachelor’s degree in a related field. Familiarity with IRB management systems (like IRBNet or Cayuse), federal compliance guidelines, and relevant certifications such as CIP (Certified IRB Professional) are typically required. Attention to detail, critical thinking, and effective written and verbal communication skills help distinguish top performers in this role. These skills are crucial for ensuring ethical research practices, regulatory compliance, and the protection of research participants.

What is the difference between Contractual Irb Analyst vs Clinical Research Coordinator?

AspectContractual Irb AnalystClinical Research Coordinator
CredentialsBachelor's degree, IRB-related certificationsBachelor's degree, clinical research training
Work EnvironmentIRB offices, regulatory agenciesResearch sites, hospitals, clinics
Employer & IndustryResearch institutions, biotech companiesHospitals, research centers
Job FocusIRB review, compliance, regulatory documentationParticipant recruitment, study coordination

The Contractual Irb Analyst primarily focuses on IRB review and regulatory compliance, working closely with research protocols and ethics boards. In contrast, a Clinical Research Coordinator manages participant recruitment and day-to-day study activities. Both roles require knowledge of clinical research processes but differ in their specific responsibilities and work environments.

What are Contractual IRB Analysts?

Contractual IRB Analysts are professionals hired on a contract basis to review research proposals and ensure that they comply with ethical standards set by Institutional Review Boards (IRBs). Their primary responsibility is to protect the rights and welfare of human research participants by evaluating study protocols, consent forms, and supporting documentation. They often work for universities, hospitals, or research organizations, and may provide expertise on federal regulations, ethical guidelines, and institutional policies. As contractors, their assignments may be project-based or for a specified period, depending on the organization's needs.

What are some common challenges a Contractual IRB Analyst might face when working with diverse research protocols?

A Contractual IRB Analyst often reviews a wide variety of research protocols, each with unique ethical and regulatory considerations. One common challenge is ensuring compliance with federal regulations while balancing the needs and timelines of researchers, especially when protocols are complex or involve vulnerable populations. Additionally, given the contractual nature of the role, analysts may need to quickly adapt to different institutional policies and communicate effectively with IRB members, researchers, and compliance staff. Staying organized and up-to-date with evolving guidelines is essential for success in this position.
More about Contractual Irb Analyst jobs
What cities are hiring for Contractual Irb Analyst jobs? Cities with the most Contractual Irb Analyst job openings:
What are the most commonly searched types of Irb Analyst jobs? The most popular types of Irb Analyst jobs are:
What states have the most Contractual Irb Analyst jobs? States with the most job openings for Contractual Irb Analyst jobs include:
Infographic showing various Contractual Irb Analyst job openings in the United States as of July 2026, with employment types broken down into 85% Full Time, 5% Part Time, 5% Temporary, and 5% Contract. Highlights an 81% In-person, and 19% Remote job distribution.
Clinical Research Financial Analyst

Full-time

Medical, Retirement, PTO

Posted 10 days ago


University Of Chicago rating

8.1

Company rating: 8.1 out of 10

Based on 47 frontline employees who took The Breakroom Quiz

152nd of 612 rated colleges and universities


Job description

Department

BSD OCR - Research Compliance


About the Department

The Office of Clinical Research (OCR) was created to further the missions of the University of Chicago Biological Sciences Division and the University of Chicago Medical Center by developing and supporting specific infrastructure components related to clinical and translational research. To provide the highest level of support and resources, the Office of Clinical Research is divided into two groups- the Institutional Review Board Administrative Staff (IRB) and the Research Operations and Conduct group (ROC). The OCR focuses on six key areas of service including: Human Subject Protection (IRB); Training and Education; Regulatory and Contract Oversight; Quality Assurance/Reporting and Auditing; Financial/Billing Compliance; Institutional Infrastructure.


Job Summary

The job provides professional support and solves straightforward problems in projects related to revenue cycle operations, including activities related to charging, billing, and collecting. Coordinates the management of successful billing and compliance activities with department managerial and executive staff.
The Clinical Research Financial Analyst is an integral member of the Office of Clinical Research. Under the direction of the Associate Director Research Billing Compliance, the Clinical Research Financial Analyst will promote and facilitate a culture of financial compliance through the regulatory and financial amendments to clinical research studies to ensure institutional adherence with Federal, State, and Local Regulations and Guidelines.
Activities include but are not limited to supporting research revenue cycle management through research billing review, processing payments, reviewing and preparing research billing documentation, and producing research financial reporting, as well as department projects and initiatives to support research billing compliance tasks as needed.

Responsibilities

  • Perform all research billing activities including, but not limited to: daily charge review, billing issue resolution, reconciliation and payment of research accounts.

  • Conduct research billing quality assurance activities, such as individual patient billing audits, study audits, device audits and validation of data and information contained within institutional systems (e.g. Epic, IRB system, clinical trial management system, etc.).

  • Assist in the development and design of training and resource materials related to research billing and financial management in collaboration with others in the office.

  • Follow standard operating procedures and policies to ensure compliant research billing as mandated by regulatory agencies (FDA, OHRP, OIG, CMS).

  • Has a moderate/solid understanding of coding procedures, workflow issues, billing infrastructure, and performance of Clinical Revenue staff.

  • Generates Epic and CTMS reports for analysis, monitoring and improving research billing metrics and processes.

  • Effectively collaborates with Clinical Trial Financial Group, Hospital Revenue Cycle team, study teams, research subjects, IRB, and other stakeholders to address research billing challenges.

  • Ensure institutional research billing compliance with Medicare's Clinical Trial Policy, federal regulations, and contractual agreements.

  • Maintain an understanding of Medicare's Clinical Trial Policy (NCD 310.1) and related guidance documents.

  • Assist in developing and maintaining polices, SOPs & SOWs related to clinical research billing process.

  • Stays current on all internal processes related to research billing, Medicare, National and local, regulations and guidelines, policies and procedures governing Research billing.

  • Prioritizes chart documentation and maintaining requirements within the department. Ensures all processes involved in accurately posting professional fees.

  • Has a moderate/solid understanding of coding procedures, workflow issues, billing infrastructure, and performance of Clinical Revenue staff. Informs department administrators, physicians, and Coder/Abstractors of regulatory changes.

  • Participates and may lead in training sessions, performing audits, and promoting an understanding of procedures, policies, and expectations in promotion of compliance efforts.

  • 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 in finance, accounting, business administration, or health information management.

Experience:

  • 2-4 years' experience with healthcare clinical research billing preferably in academic medical setting, clinical research management, health system operations.

  • Experience with Epic Research Billing functions.

  • Experience with a Clinical Trial Management system (CTMS) preferably OnCore, financial software, ERP systems.

  • Accounting and finance experience strongly preferred.

Preferred Competencies

  • Knowledge of the Medicare Clinical Trials Policy and other federal, state and institutional clinical research regulations.

  • Expertise in CPT, Modifiers, ICD, and HCPCS codes to support billing and compliance efforts.

  • Strong knowledge of clinical trial contracting, revenue recognition principles, and relevant regulatory guidelines (e.g., ICH-GCP).

  • Excellent attention to detail and analytical skills, with a focus on accuracy in financial operations.

  • Strong communication and interpersonal skills for effective collaboration with cross-functional teams and external partners.

  • Expertise in Microsoft Excel.

  • Excellent Written and verbal communication skills.

  • Strong investigative and problem-solving skills.

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) MUSTbe 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

$70,000.00 - $95,000.00

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.


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