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Full Time Remote Clinical Trials Jobs (NOW HIRING)

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 ...

Summary This position will be on site/remote This will be for our Lymphoma/Myeloma team. Position ... the Clinical Trials Business Office and Research Finance to coordinate budget development and ...

Summary This position will be on site/remote This will be for our Hematology/Myeloid team. Position ... the Clinical Trials Business Office and Research Finance to coordinate budget development and ...

Remote Clinical Counselor

$60K - $80K/yr

Monday - Friday, 7:00am - 4:00pm Japan Standard Time / Sunday - Thursday, 6:00pm - 3:00am Eastern Time Summary The Remote Clinical Counselor works as a full-time employee of Zeiders Enterprises and ...

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Full Time Remote Clinical Trials information

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$28

$62

$96

How much do full time remote clinical trials jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for full time remote clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is the difference between Full Time Remote Clinical Trials vs Full Time Remote Clinical Research Coordinators?

AspectFull Time Remote Clinical TrialsFull Time Remote Clinical Research Coordinators
CredentialsTypically requires a degree in life sciences, nursing, or related fields; certifications like CCRP are commonSimilar credentials, often with certifications like CCRP or CRC
Work EnvironmentConducts or oversees clinical trials remotely, often collaborating with sites and sponsorsCoordinates trial activities, manages data, and communicates with sites remotely
Industry UsageUsed by pharmaceutical companies, CROs, and research institutionsCommonly employed by research organizations and sponsors for trial management

Both roles involve remote work in clinical research, requiring similar credentials and industry usage. Full Time Remote Clinical Trials focus on overseeing or conducting entire trials, while Clinical Research Coordinators handle day-to-day trial coordination and data management. Understanding these differences helps job seekers find the right fit in the remote clinical research field.

More about Full Time Remote Clinical Trials jobs
What cities are hiring for Full Time Remote Clinical Trials jobs? Cities with the most Full Time Remote Clinical Trials job openings:
What are the most commonly searched types of Remote Clinical Trials jobs? The most popular types of Remote Clinical Trials jobs are:
What states have the most Full Time Remote Clinical Trials jobs? States with the most job openings for Full Time Remote Clinical Trials jobs include:
Infographic showing various Full Time Remote Clinical Trials job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 8% In-person, and 92% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trials Coverage Analyst

Vitalief

Chicago, IL • 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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