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Remote Clinical Trials Data Analyst Jobs (NOW HIRING)

... remote capacity, supporting a leading academic clinical research center in Chicago. The ideal ... Proficiency in document and data management tools, including Microsoft Word, Excel, PowerPoint ...

Clinical Data Manager

Austin, TX ยท Remote

$125K - $175K/yr

... active clinical trials. This individual will play a critical role in ensuring high-quality ... Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical ...

Clinical Data Manager

Austin, TX ยท Remote

$125K - $175K/yr

... active clinical trials. This individual will play a critical role in ensuring high-quality ... Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical ...

... data and analysis infrastructure platforms and other technical solutions to support the data flow from data collection to data submission. Using expertise in R programming and clinical trials to ...

Your Impact Set strategic direction and lead large clinical trials/data collection efforts ... Manage the operational, analytical, fiscal and logistical tasks associated with our clinical ...

This position's work location is fully remote with occasional time on-campus in Boston, MA. The ... Support the clinical programs with outcomes data collection, reporting, analysis and audits

Our global team of experts - spanning psychology, data science, operations, and technology - works ... This role will require an analytical and flexible mindset and extensive communication and ...

Summary This position will be on site/remote This will be for our Lymphoma/Myeloma team. Position ... data specialists) Takes the lead and/or participates in development and execution oftraining ...

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Remote Clinical Trials Data Analyst information

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How much do remote clinical trials data analyst jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for remote clinical trials data analyst in the United States is $36.36, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $42.07 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Trials Data Analyst vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trials Data AnalystRemote Clinical Research Coordinator
Primary RoleAnalyzes clinical trial data, manages databases, generates reportsCoordinates trial activities, manages site operations, ensures protocol compliance
Required SkillsData analysis, statistical software, attention to detailCommunication, organization, regulatory knowledge
Work EnvironmentRemote, primarily computer-basedRemote or onsite, site management
Common CertificationsCertified Clinical Data Manager (CCDM), related data certificationsCertified Clinical Research Professional (CCRP), site management certifications

The Remote Clinical Trials Data Analyst focuses on analyzing and managing clinical data remotely, while the Remote Clinical Research Coordinator handles trial coordination and site management. Both roles require understanding of clinical research but differ in daily tasks and skill sets.

More about Remote Clinical Trials Data Analyst jobs
What cities are hiring for Remote Clinical Trials Data Analyst jobs? Cities with the most Remote Clinical Trials Data Analyst job openings:
What are the most commonly searched types of Clinical Trials Data Analyst jobs? The most popular types of Clinical Trials Data Analyst jobs are:
What states have the most Remote Clinical Trials Data Analyst jobs? States with the most job openings for Remote Clinical Trials Data Analyst jobs include:
Infographic showing various Remote Clinical Trials Data Analyst job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 88% Full Time, 6% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 7% Hybrid, and 10% Remote job distribution, with an average salary of $75,625 per year, or $36.4 per hour.

Clinical Trials Coverage Analyst

Vitalief

Chicago, IL โ€ข Remote

$70K - $85K/yr

Full-time

Re-posted 26 days ago


Job description

ABOUT VITALIEF
Vitalief is a consulting and professional services firm that partners with clinical research sites, sponsors, and CROs to improve trial activation, operational performance, and workforce readiness. By combining clinical research expertise with operational and business excellence, we help organizations streamline processes, reduce costs, accelerate timelines, and enhance patient outcomes.
THE ROLE
We are seeking a full-time, fully benefited Vitalief employee to serve as a Clinical Trials Coverage Analyst in a fully remote capacity, supporting a leading academic clinical research center in Chicago. The ideal candidate brings strong expertise in Medicare billing guidelines, clinical trial operations, experience working on Oncology protocols, and OnCore calendar builds, and will ensure compliance while supporting clinical trial billing operations and advising key stakeholders.
WHY VITALIEF? 
  • Work remotely while supporting high-impact clinical trials.
  • Be a key contributor to billing compliance and operational excellence.
  • Collaborate with experienced clinical trial teams and expand your expertise in Medicare coverage and OnCore systems.
  • Transition seamlessly from a Vitalief employee after 6 months to a permanent employee of our client organization.
  • Market-competitive salary: $70,000 to $85,000 depending on experience level.

KEY RESPONSIBILITIES
  • Conduct Medicare Coverage Analyses (MCA) for a mixture of oncology and non-oncology clinical trial protocols identifying which procedures and services are billable to Medicare versus those considered research related.
  • Review clinical trial protocols, schedules of events, and informed consent forms to ensure billing compliance with CMS regulations.
  • Develop, maintain, and validate OnCore calendar builds for clinical trial visits, procedures, and study milestones.
  • Collaborate with cross-functional teams including Clinical Operations, Finance, Regulatory, and Study Teams to provide guidance and clarification on coverage decisions.
  • Prepare and maintain coverage analysis documentation, summary tables, and billing justification reports for both internal and external stakeholders.
  • Serve as a subject matter expert for Medicare coverage rules, assisting study teams in identifying potential billing risks and providing actionable recommendations.
  • Support internal and external audits, ensuring all coverage decisions are well-documented and compliant with federal and sponsor requirements.
  • Keep current with CMS updates and industry best practices, applying knowledge to optimize coverage analyses and study operations.

QUALIFICATIONS
  • Bachelor’s degree in Healthcare Administration, Medical Coding, Auditing, Finance, Accounting, Nursing, or a related field. 
  • Minimum 3 years of Medicare Coverage Analysis experience in clinical research or healthcare billing.
  • Must have experience working on oncology clinical trial protocols.
  • Hands-on experience developing, maintaining, and validating OnCore calendar builds for clinical trial visits, procedures, and study milestones is preferred – but not required as training will be provided.
  • Strong understanding of CMS guidelines, Medicare billing compliance, and clinical trial operations.
  • Demonstrated ability to work independently and manage multiple protocols and deadlines simultaneously.
  • Exceptional attention to detail, analytical skills, and problem-solving abilities.
  • Strong written and verbal communication skills, with the ability to explain complex billing concepts to non-technical stakeholders.
  • Comfortable working in a fully remote environment, collaborating effectively with distributed teams across multiple locations.
  • Proficiency in document and data management tools, including Microsoft Word, Excel, PowerPoint, Adobe, Teams, and SharePoint.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs.
IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
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