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Remote Clinical Research Coverage Analyst Jobs (NOW HIRING)

$77K - $90K/yr

The Medicare Coverage Analyst (MCA) is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-related documents to create a ...

... Analyst role for our company. We are based in India and USA and this position will be fully remote ... various clinical research related tasks and requirements. Some understanding of basic medical ...

Remote Duration: Direct Hire FTE Must Have's: * Bachelor's Degree in Health Information Management ... Analyzing and optimizing clinical workflows to improve efficiency and patient outcomes Summary: The ...

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Remote Clinical Research Coverage Analyst information

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$38.5K

$74K

$99.5K

How much do remote clinical research coverage analyst jobs pay per year?

As of Aug 18, 2026, the average yearly pay for remote clinical research coverage analyst in the United States is $73,965.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,000.00 and $98,500.00 per year, depending on experience, location, and employer.

What is a remote clinical research coverage analyst?

Remote Clinical Research Coverage Analysts are professionals who evaluate clinical research studies to determine which procedures and services are billable to insurance, sponsors, or research grants, all while working remotely. They review study protocols, informed consent documents, and payer policies to ensure compliance with regulations and institutional guidelines. Their work is critical in helping research organizations and hospitals avoid billing errors and maintain financial integrity for clinical trials. By working remotely, they leverage digital tools and secure systems to access and analyze study documents from any location.

What are the key skills and qualifications needed to thrive as a remote clinical research coverage analyst?

To thrive as a Remote Clinical Research Coverage Analyst, you need a solid understanding of clinical research billing, healthcare compliance regulations, and medical terminology, often supported by a bachelor’s degree in a health-related field. Familiarity with billing systems, electronic medical records (EMRs), Medicare Coverage Analysis (MCA) tools, and relevant certifications such as CCRC or ACRP are commonly required. Attention to detail, analytical thinking, and strong written communication help ensure accuracy and effective collaboration with remote teams. These skills and qualifications are crucial for ensuring regulatory compliance, minimizing financial risk, and supporting successful clinical trial operations.

How does a remote clinical research coverage analyst collaborate with clinical trial teams and ensure accurate coverage analysis from a distance?

As a Remote Clinical Research Coverage Analyst, you will frequently interact with study coordinators, investigators, billing teams, and compliance officers via virtual meetings, emails, and shared project management systems. Even though you work remotely, you are expected to review clinical trial protocols, determine qualifying status, and analyze billing grids to ensure that all patient care costs are accurately classified as either standard of care or research-related. Clear communication and strong organizational skills are essential to coordinate effectively, resolve discrepancies, and keep all stakeholders informed about regulatory and payer requirements. Regular updates and virtual check-ins with site teams help maintain alignment and ensure ongoing compliance.

What is the difference between Remote Clinical Research Coverage Analyst vs Remote Clinical Trial Coordinator?

AspectRemote Clinical Research Coverage AnalystRemote Clinical Trial Coordinator
Required CredentialsTypically requires a background in healthcare, clinical research certifications, and knowledge of coverage policiesRequires clinical trial management experience, good organizational skills, and often a degree in health sciences or related fields
Work EnvironmentPrimarily remote, focusing on coverage analysis, documentation, and complianceRemote or hybrid, coordinating trial activities, patient recruitment, and site communication
Employer & Industry UsagePharmaceutical companies, insurance providers, CROsResearch institutions, pharmaceutical companies, CROs

The Remote Clinical Research Coverage Analyst primarily focuses on evaluating insurance coverage and reimbursement policies for clinical trials, ensuring compliance and proper billing. In contrast, the Remote Clinical Trial Coordinator manages trial logistics, patient coordination, and site communication. Both roles are essential in clinical research but differ in their core responsibilities and skill sets.

More about Remote Clinical Research Coverage Analyst jobs

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Cities with the most Remote Clinical Research Coverage Analyst job openings:

What are the most commonly searched types of Clinical Research Coverage Analyst jobs?

The most popular types of Clinical Research Coverage Analyst jobs are:

What states have the most Remote Clinical Research Coverage Analyst jobs?

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

What job categories do people searching Remote Clinical Research Coverage Analyst jobs look for?

The top searched job categories for Remote Clinical Research Coverage Analyst jobs are:

Infographic showing various Remote Clinical Research Coverage Analyst job openings in the United States as of August 2026, with employment types broken down into 79% Full Time, 13% Part Time, 3% Temporary, and 5% Contract. Highlights an 3% In-person, and 97% Remote job distribution, with an average salary of $73,965 per year, or $35.6 per hour.

Clinical Research Coverage Analyst

The University of Chicago

Chicago, IL • On-site, Remote

$65K - $90K/yr

Full-time

Medical, Retirement, PTO

Re-posted 3 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

162nd of 618 rated colleges and universities


Job description

Department
BSD OCR - CTMS Support Unit
About the Department
The Office of Clinical Research (OCR) is dedicated to supporting the infrastructure for the management and administration of clinical research at The University of Chicago as well as individual research programs with the goal of improving communication, consistency, and collaboration across the Biological Sciences Division and UChicago Medicine.
To mission of the OCR is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers.
Job Summary
The job maintains regulatory compliance programs, including the interpretation of systems to identify areas of risk and may coordinate internal audits. With a moderate level of direction, participates in compliance documentation, compliance training, and compliance committee formation.
The Coverage Analyst is dedicated to ensuring billing compliance for clinical research and supports utilization of the Clinical Trial Management System (CTMS), Oncore. The Coverage Analyst plays a crucial role in evaluating clinical research protocols, informed consent forms, clinical trial budgets, and other pertinent study documents to generate a protocol calendar in the CTMS system and develop coverage analysis/billing grid. The Coverage Analyst specifies which procedures and services may qualify as 'Routine Cost' and be billable to patient insurance, and which should be charged to the study. The Coverage Analyst is responsible for determining whether proposed clinical research studies meet the criteria for a Qualifying Clinical Trial as defined by the Medicare Clinical Trial Policy (NCD 310.1). As a member of the Research Systems & Coverage Analysis (RSCA) Unit, within the Office of Clinical Research, the Coverage Analysts works as part of a team to support and optimize clinical trial initiation and financial workflows, partnering closely with research teams and key stakeholders in the process.
Responsibilities
  • Reviews clinical trial protocols, budgets, contracts, and informed consent documents to inform billing designations.
  • Creates detailed coverage analyses that outline the billing of clinical items and services required by research studies.
  • Develops study calendars within the Clinical Trial Management System, Oncore.
  • Ensures consistency in the application of Medicare and other applicable rules across studies and alignment of study documents with billing regulations.
  • Works collaboratively with key offices, including the Human Research Protection Program and research units, to harmonize regulatory and budgetary processes in clinical trials.
  • Communicates the results of coverage analyses to principal investigators and/or study teams, providing detailed explanations and addressing any questions or concerns.
  • Ensures that coverage analyses outputs are reviewable and auditable for quality and compliance.
  • Recruits, onboards, and trains new clinical research staff to ensure adherence to billing compliance procedures.
  • Coordinates department or clinic compliance with a moderate level of guidance.
  • Prepares, completes and submits all compliance documentation on a routine basis. Coordinates compliance committee meetings.
  • 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.

Experience:
  • Clinical research experience such as clinical research conduct, regulatory compliance, or related research activities.
  • Coverage analysis experience.

Preferred Competencies
  • Interpret research protocols, budgets, and consent forms to extrapolate billing/coverage information.
  • Problem-solve, leveraging information and expertise available.
  • Strong organizational skills.
  • Manage projects at various stages of completion.
  • Manage high volume of workload and meet deadlines.
  • Demonstrated attention to detail.

Working Conditions
  • Office environment.

Application Documents
  • Resume (required)
  • Cover Letter (preferred)

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) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
Job Family
Legal & Regulatory Affairs
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
$65,000.00 - $90,000.00
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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