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100% Remote Clinical Trial Coverage Analyst

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 
Illinois (USA), United States

Offer summary

Qualifications:

Minimum of 3 years coverage analysis experience, Strong reading comprehension and critical thinking skills, Proficiency in Excel for analysis templates, Knowledge of clinical research and medical terminology.

Key responsabilities:

  • Conduct comprehensive coverage analysis of clinical trial protocols
  • Communicate analysis results to Principal Investigators and study teams
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Job description

Job Title: 100% Remote Clinical Trial Coverage Analyst

Job Location: Chicago, IL, USA

Job Location Type: Remote

Job Contract Type: Full-time

Job Seniority Level: Mid-Senior level

Employer Industry: Clinical Research and Talent Solutions

Why Consider This Job Opportunity

  • Fully remote position, allowing for flexibility in work location
  • Opportunity for career advancement and growth within the organization
  • Collaborative and communicative work environment with a strong emphasis on teamwork
  • Engage in meaningful work that supports clinical research and regulatory compliance
  • Company committed to diversity, equity, and inclusion in the workplace

What To Expect (Job Responsibilities)

  • Conduct comprehensive coverage analysis by reviewing clinical trial protocols and related regulatory documents
  • Create and communicate coverage analysis results to Principal Investigators and study teams
  • Interpret research contracts, study budgets, clinical protocols, and consent forms to determine billing and coverage data
  • Outline billing of clinical items and services required by research studies
  • Ensure compliance with federal and state billing regulations, including Medicare's National Coverage Decision (NCD) 310.1

What Is Required (Qualifications)

  • Minimum of 3 years of recent coverage analysis experience
  • Strong reading comprehension skills and critical thinking ability
  • Proficiency in Excel for building analysis templates
  • Knowledge of clinical research, including commercial, federal, and PI-initiated protocols
  • Familiarity with medical terminology and regulatory compliance guidelines

How To Stand Out (Preferred Qualifications)

  • Experience with clinical trials research activities and IRB informed consent guidelines
  • Resourcefulness, humility, flexibility, and the ability to accept feedback

#ClinicalResearch #RemoteWork #CareerGrowth #DiversityAndInclusion #HealthcareCompliance

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https://lifelancer.com/jobs/view/eb62d9cdfc4080f6e0e9712eb127941f

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Information Technology & Services
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Microsoft Excel
  • Critical Thinking
  • Reading Comprehension
  • Physical Flexibility
  • Humility
  • Resourcefulness

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