Research Billing Compliance Analyst

Yale Cancer Center; New Haven, Northern (CT, KY); Hybrid; USD 65,000 - 101,000; Full time

Job summary

Yale Cancer Center's Clinical Trials Office seeks a Research Billing Compliance Analyst to act as the primary liaison between hospital and professional billing offices. You will review charges, ensure CMS regulatory alignment, maintain documentation, and communicate findings to stakeholders.

You will collaborate with clinical research staff, investigators and vendors to support policy development, process improvements, and training in research billing compliance while staying current with

Qualifications

• Experience with regulatory documents such as MCA and CTA.
• Strong communication and organizational skills with attention to detail.
• Ability to prioritize tasks in a fast-paced environment.
• Experience working with clinical trial systems and protocols.
• Proficiency with Microsoft Office and clinical trial platforms.

Responsibilities

• Complete risk assessments on trials with billable services using CTMS/OnCore.
• Evaluate ICD-10, CPT-4, HCPCS codes and modifiers for compliance.
• Identify charges not defined in protocols and coordinate with Sponsored Projects.
• Review billable services in OnCore and Epic; communicate with Compliance.
• Develop corrective action plans with PIs and study teams; implement changes.
• Maintain logs of investigations; enter findings in OnCore; analyze trends.
• Assist in research billing training; develop materials on coding and regs.
• Generate OnCore reports to identify trends and focus reviews.
• Support implementation of the Research Billing Compliance Program.
• Stay current with coding best practices and regulatory changes; maintain CPC CEUs.

Skills

Clinical trial systems

Regulatory documents (MCA, CTA)

Verbal and written communication

Prioritization & multitasking

MS Office

Education

Oncology trials experience

Tools

OnCore

Epic

CTMS

Job description

Salary Range

$65,000.00 - $101,000.00

Job Requisition ID

138519WD

Overview

Reporting to the Director of Operations at the Yale Cancer Center Clinical Trials Office, the Research Billing Compliance Analyst is the primary liaison with the centralized hospital and professional billing offices. This role receives charges from these two offices for review and determination of appropriate billing designations, ensuring alignment with Medicare (CMS) regulations and institutional policies. The analyst maintains detailed records, monitors trends and risk areas, and communicates findings to relevant stakeholders. Collaborating with clinical research staff, investigators, vendors, and administrators, the analyst supports policy development and process improvements to enhance billing compliance. Additional responsibilities include resolving billing discrepancies, staying current with federal regulations and best practices, and serving as a key resource and liaison for clinical trial billing. The analyst also contributes robust documentation and follow-up related to clinical trials billing within the Clinical Trial Management System.

Required Skills and Abilities

• 1. Demonstrated ability with using clinical trial systems, protocol tracking and reporting. Advanced knowledge and experience with clinical trial regulatory documents such as protocols, informed consent documents, Medicare Coverage Analysis (MCA), and Clinical Trial Agreements (CTA).
• 2. Outstanding verbal, written, communication and organizational skills, exceptional attention to detail, well-developed analytical and problem-solving skills, demonstrated superior customer service abilities and outstanding time management skills.
• 3. Ability to possess sound, independent judgement, with ability to prioritize and handle many tasks simultaneously in a complex, fast-paced environment.
• 4. Ability to work independently and effectively with a wide range of individuals.
• 5. Strong computer skills required, including strong competency in Microsoft Office programs (Word, Excel, PowerPoint, etc.).

Preferred Education/Experience

Experience working with oncology clinical trials; Medicare Coverage Analysis. Prior experience as a Clinical Research Coordinator or Clinical Research Nurse highly preferred.

Principal Responsibilities

• 1. Primary responsibilities include the completion of risk assessments on all MQT trials with billable services. The level of risk is determined utilizing the CTMS (OnCore) risk assessment tool as well as the clinical trial documentation and information provided within the study’s protocol. Once the risk assessment is complete and all trials scored, random selection of the highest risk trials will be assessed and reviewed for accurate research billing compliance and proper medical documentation.
• 2. Medical documentation, coding and billing will be evaluated for accurate ICD-10, CPT-4, HCPC and modifier placement in compliance with University and government regulations.
• 3. Identify potential clinical research charges not specifically defined in research protocols. Work collaboratively with the Office of Sponsored Projects to determine proper documentation alignment including but not limited to the informed consent forms, research protocols, clinical trial agreement and trials finalized budget.
• 4. Review all billable services/encounters for designated studies utilizing OnCore and Epic. Communicate and supply YNHHS Compliance department with ongoing reviews and assist with any information requested in order to ensure accurate and consistent billing for both professional and hospital charges.
• 5. Evaluate findings, identify system control weaknesses and in conjunction with department management, assist in the development of a corrective action plan for Principal Investigator and study team. Assist in the implementation and follow up of all corrective action changes.
• 6. Maintain accurate logs, including spreadsheets, of all ongoing investigations. Enter all review findings in the OnCore registry database Identify and analyze any trends and report findings to the Associate Director, Research Billing Compliance.
• 7. Assist in the conduction of research training sessions with Principal Investigators and research related study teams and personnel. Provide subject matter expertise and input on areas where education is needed. Assist in the development of training materials and programs for research billing compliance, including but not limited to accurate coding, documentation billing and regulatory guidelines.
• 8. Conduct data analysis. Generate reports using OnCore reporting tools to identify trends and problem areas for focus of internal reviews.
• 9. Assist and support with the ongoing implementation of the Research Billing Compliance Program as well as knowledge retention and maintenance of the Yale School of Medicine’s Research Billing Compliance Plan, operations and procedures.
• 10. Stay abreast of best practice coding and billing initiatives as well as all pertinent regulatory changes. Maintain CPC designation by obtaining necessary CEUs on an annual basis.

Required Education and Experience

Bachelor’s Degree in Health or Business Administration or a related field and 3 years of experience working directly with clinical research charge review and billing or an equivalent combination of education and experience.

Original Job Posting Date

09/23/2026

Job Category

Professional

Bargaining Unit

NON

Compensation Grade

Clinical & Research

Compensation Grade Profile

Research Billing Compliance Analyst (23)

Time Type

Full time

Duration Type

Staff

Work Model

Remote

Location

221 Whitney Ave, New Haven, Connecticut

Background Check Requirements

All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks basedon the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.

Health Requirements

Certain positions have associated health requirements based on specific job responsibilities. These may include vaccinations, tests, or examinations, as required by law, regulation, or university policy.

Posting Disclaimer

The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific dutiesand responsibilities of the position. Employees will be assigned specific job-related duties throughtheir hiring department.
University policy is committed to affirmative action under law in employment of women, minority group members, individuals with disabilities, and protected veterans. Additionally, in accordance with Yale's Policy Against Discrimination and Harassment, and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual's sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran.
Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).

Note

Yale University is a tobacco-free campus.