Clinical Research Billing Analyst

Vitalief•New Brunswick, NJ

3d•$75,000 - $100,000•Remote

About The Position

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. 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.

Requirements

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.

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.