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Remote Clinical Trials Data Analyst Jobs in Edison, NJ

Remote Duration 4-6 months The RBQM Data Scientist supports central monitoring and risk-based ... for clinical trials. This role focuses on implementing and running pre-defined KRIs, QTLs, and ...

... performing remote clinical activities in compliance with study protocols, Standard Operating ... Collect, maintain, and securely storeall relevant data associated with clinical research trials in ...

Data Analyst Location: Remote Top Skills: * Python * Tableu * SQL Strong * AWS Job Requirement: * * Need to have experience with Data sets to do: * Gain customer insights (segmentation and ...

In this role, the Data Analyst (Remote) will be responsible for ensuring the business makes better decisions through collection and usage of data. Responsibilities: The Data Analyst (Remote) will:

Data Analyst

New York, NY · Remote

$55 - $60/hr

This is a remote opportunity. About this Position Join a fast-paced Product Operations team focused ... Analyze operational data to identify trends, risks, and improvement opportunities * Build and ...

Data Analyst

New York, NY · Remote

$55 - $60/hr

This is a remote opportunity. About this Position Join a fast-paced Product Operations team focused ... Analyze operational data to identify trends, risks, and improvement opportunities * Build and ...

Over the past two years, our team of 3 has become a fully remote team of 30+ Butter Slices, spread ... As Arsenaults Data Analyst, youll play a leading role in helping us answer strategic business ...

Data Analyst

New York, NY · On-site +1

$97K/yr

Remote, New York City, or Oakland, CA * Travel is encouraged approximately once every 6 months to ... Our Data Analysts work with diverse data - criminal justice data both raw and processed from across ...

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Remote Clinical Trials Data Analyst information

See Edison, NJ salary details

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

As of Sep 8, 2026, the average hourly pay for remote clinical trials data analyst in Edison, NJ is $37.64, according to ZipRecruiter salary data. Most workers in this role earn between $30.38 and $43.56 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.

What are popular job titles related to Remote Clinical Trials Data Analyst jobs in Edison, NJ?

For Remote Clinical Trials Data Analyst jobs in Edison, NJ, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Trials Data Analyst jobs in Edison, NJ look for?

The top searched job categories for Remote Clinical Trials Data Analyst jobs in Edison, NJ are:

Clinical Trials Medicare Coverage Analyst

Vitalief

New Brunswick, NJ • On-site, Remote

$75K - $100K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 24 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 Medicare Coverage Analyst in a fully remote capacity, supporting Vitalief's client, a leading academic clinical research center in the Chicago area. 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 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: This is a 100% remote position.
  • Salary Range: $75,000 to $100,000 - Based 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 supporting clinical research studies for an Academic Medical Center (AMC) or health (hospital) system.
  • 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.