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Clinical Research Billing Analyst Jobs (NOW HIRING)

The Analyst collaborates with Clinical Trial Finance, Revenue Cycle, Research Operations, study teams, investigators, IRB, and other stakeholders to resolve billing issues, improve processes, and ...

New

The Analyst collaborates with Clinical Trial Finance, Revenue Cycle, Research Operations, study teams, investigators, IRB, and other stakeholders to resolve billing issues, improve processes, and ...

New

Billing Analyst

Melville, NY ยท Hybrid

$62K - $69K/yr

... analysis, billing, collections, and working in a collaborative environment ... You will play a key role in managing the financial lifecycle of clinical research studies while ...

New

Billing Analyst

Melville, NY ยท Hybrid

$62K - $69K/yr

... analysis, billing, collections, and working in a collaborative environment ... You will play a key role in managing the financial lifecycle of clinical research studies while ...

New

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Clinical Research Billing Analyst information

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How much do clinical research billing analyst jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical research billing analyst in the United States is $39.80, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $45.67 per hour, depending on experience, location, and employer.

What is a clinical research billing analyst?

A Clinical Research Billing Analyst is a specialized professional who ensures that billing for clinical research studies complies with federal, state, and institutional regulations. They review research protocols, determine which medical services should be billed to a research sponsor versus a patient's insurance, and help prevent billing errors or fraud. Their work helps institutions maintain compliance, secure appropriate funding, and avoid costly billing mistakes in clinical trials.

How does a clinical research billing analyst collaborate with clinical teams and research coordinators to ensure compliant billing practices?

A Clinical Research Billing Analyst works closely with clinical teams, research coordinators, and financial departments to ensure all services related to clinical trials are billed appropriately. This involves reviewing study protocols, identifying which services are billable to the study sponsor versus insurance, and clarifying billing guidelines with team members. Regular meetings and clear communication are essential to resolve discrepancies, educate staff on compliance requirements, and ensure accurate documentation throughout the research process. This collaborative approach helps minimize billing errors and supports regulatory compliance.

What are the key skills and qualifications needed to thrive as a clinical research billing analyst, and why are they important?

To thrive as a Clinical Research Billing Analyst, you need expertise in clinical research protocols, healthcare billing regulations, and a background in finance or healthcare administration, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic health records (EHRs), and knowledge of Medicare Coverage Analysis (MCA) and coding standards are typically required. Attention to detail, analytical thinking, and effective communication are vital soft skills for ensuring regulatory compliance and collaborating with research teams. These skills are essential for accurately managing research billing, preventing compliance issues, and supporting the financial integrity of clinical studies.
More about Clinical Research Billing Analyst jobs

What cities are hiring for Clinical Research Billing Analyst jobs?

Cities with the most Clinical Research Billing Analyst job openings:

What states have the most Clinical Research Billing Analyst jobs?

States with the most job openings for Clinical Research Billing Analyst jobs include:

Infographic showing various Clinical Research Billing Analyst job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $82,791 per year, or $39.8 per hour.

Clinical Research Billing Analyst

Vitalief

New Brunswick, NJ โ€ข On-site

$75K - $100K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 3 days ago

New


Job description

ABOUT VITALIEF
Vitalief is a clinical research consulting firm focused exclusively on the clinical research industry, providing consulting, staffing, and technology-enabled services to academic medical centers, health systems, sponsors, CROs, and site networks.  By combining deep subject matter expertise with the experience of senior research practitioners, we help organizations accelerate study activation, optimize operations, improve financial performance, and build scalable workforce solutions that reduce costs, increase efficiency, and advance clinical breakthroughs for patients.
The Role
As part of our growth, we are seeking a hands-on, detail-oriented, client-facing professional with clinical trial billing expertise to join Vitalief’s Clinical Research Budgeting and Billing Outsourcing Services Team. This role directly supports Vitalief’s Academic Medical Center (AMC) and health system clients with clinical research revenue cycle operations, including research billing, charge review, payment reconciliation, billing issue resolution, compliance monitoring, and financial reporting. The Analyst collaborates with Clinical Trial Finance, Revenue Cycle, Research Operations, study teams, investigators, IRB, and other stakeholders to resolve billing issues, improve processes, and ensure accurate, compliant research revenue cycle operations.
Why Join Vitalief?
  • Make an Impact: Support leading AMCs and health systems in improving clinical trial financial performance and compliance.
  • Innovation-Driven: Help modernize clinical trial budgeting and billing processes using technology and best practices.
  • People-First Culture: Thrive in an environment that fosters growth, innovation, and collaboration.
  • Comprehensive Benefits: Enjoy 20 PTO days, 9 paid holidays, company-paid life insurance, short- and long-term disability, a 401(k)-retirement plan, and robust healthcare options.
  • Flexible & Remote-Friendly: Primarily remote with occasional travel (up to 10%).
  • Salary Range: $75,000 to $110,000 – Based on experience level.

Responsibilities
  • Perform daily clinical research billing, charge review, reconciliation, payment processing, and issue resolution.
  • Review research charges against study budgets, clinical trial agreements, coverage requirements, and institutional policies.
  • Conduct patient, study, and device billing audits and quality assurance reviews.
  • Validate research billing data across Epic, CTMS, IRB, and financial systems.
  • Support compliance with Medicare's Clinical Trial Policy (NCD 310.1) and applicable regulatory requirements.
  • Investigate and resolve billing, coding, reconciliation, and workflow discrepancies.
  • Generate and analyze Epic, CTMS, and financial reports to monitor billing activity and performance.
  • Prepare billing documentation, financial reports, reconciliations, and supporting analyses.
  • Develop and maintain research billing policies, SOPs, workflows, and training materials.
  • Monitor regulatory and Medicare updates and communicate changes to relevant stakeholders.
  • Collaborate with Research, Finance, Revenue Cycle, Coding, IRB, and study teams to resolve issues and improve processes.
  • Support billing audits, training, process improvement initiatives, and other research revenue cycle projects.

Qualifications
  • Bachelor's degree in Finance, Accounting, Business Administration, Health Information Management, Healthcare Administration, Clinical Research, or related field.
  • 2 to 4 years of experience in clinical research billing, healthcare revenue cycle, research financial operations, or health system operations.
  • Experience in an academic medical center or health system preferred.
  • Experience with Epic research billing and a clinical trial management system such as OnCore, Veeva Vault, Clinical Conductor, etc.
  • Knowledge of Medicare Clinical Trial Policy (NCD 310.1) and clinical research billing compliance requirements.
  • Knowledge of CPT, HCPCS, ICD, modifiers, coding, and healthcare billing practices.
  • Understanding of clinical trial budgets, coverage requirements, agreements, revenue recognition, and research billing processes.
  • Experience with billing audits, quality assurance, financial reconciliation, and compliance reviews.
  • Strong analytical, investigative, problem-solving, and Microsoft Excel skills.
  • Ability to generate, interpret, and analyze data from Epic, CTMS, financial, and other institutional systems.
  • Excellent communication, collaboration, organizational, and time-management skills.
  • Ability to work independently and effectively in a primarily remote environment while managing multiple priorities and deadlines.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs.  Ability to travel up to 10% domestically.
 

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