Coverage Analyst

WCG

Coverage Analyst supporting WCG’s clinical trial solutions by analyzing protocols, building activity grids, and identifying applicable CPT/HCPCS codes. Reviewing coverage-analysis work for quality.

Posted 8/18/2026full-timeRemote • North Carolina • 🇺🇸 United StatesJunior💰 $23 - $36 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial coverage analysis, including the ability to read and interpret clinical trial protocols and develop activity grids. Proficient in identifying CPT/HCPCS codes and maintaining high attention to detail in documentation and communication.

Highest-signal resume keywords

Clinical Trial Coverage AnalysisCPT/HCPCS Code IdentificationClinical Trial Protocol InterpretationProficient With ExcelExcellent Oral And Written Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial Coverage AnalysisCPT/HCPCS Code IdentificationClinical Trial Protocol InterpretationResearch Insurance BillingActivity Grid Development

Soft Skills

Attention To DetailOrganizational SkillsInvestigative SkillsInterpersonal CommunicationProactive Approach

Industry Keywords

Clinical TrialsOncologyMedical-Device TherapeuticsMedicare NCD 310.1Performance-Driven Environment

About the role

Key responsibilities & impact

Contribute to the development of clinical trial coverage analysis
Read and analyze clinical trial protocols and develop activity grids to identify required tests, procedures, and assessments
Use software and internal resources to identify potential CPT/HCPCS codes for applicable activity-grid items
Review work completed by others as part of the internal quality review process
Perform other duties as assigned by the supervisor
Maintain required attendance and punctuality

Requirements

What you’ll need

Bachelor’s degree in related field; significant work experience in the specific field may be considered in lieu of a relevant degree
At least 1 year of professional experience
Ability to work in a performance-driven environment with a proactive, results-driven, and goal-oriented approach
Demonstrated ability to learn and apply technical and scientific product-related information consultatively
Excellent attention to detail and highly organized
Ability to understand clinical terms and descriptors
Strong investigative skills; ability to read complex technical documents, synthesize relevant information, and clearly document findings
Excellent oral, written, and interpersonal communication skills
Proficient with Excel
Familiarity with the clinical trial start-up process preferred but not required
Experience interpreting clinical trial protocols to assess activity related to visit schedules and treatment plans preferred but not required
Familiarity with research insurance billing and coverage guidelines, such as Medicare NCD 310.1, preferred but not required
Experience as a clinical research coordinator, preferably in oncology or medical-device therapeutic areas, preferred but not required
Ability to meet light to moderate physical and sensory requirements, including extended sitting and frequent keyboarding
Travel requirement: 0%–5%

Benefits

Comp & perks

Comprehensive Benefits package - Health, Dental, Vision, Life Disability, 401k with match, and flexible spending accounts
Employee Assistance Programs and additional work/life resources
Referral Bonuses and Tuition Reimbursement
Paid time off including holidays, vacation, and sick time
Volunteer Time Off to benefit the community
Opportunities for career development with on-the-job training, certification assistance, and continuing education reimbursement