Coverage Analyst

🕒 August 18

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $23 - $36 / hour

⏰ Full Time

🟢 Junior

🧐 Analyst

👻 Ghost score 6%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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WCG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💊 Pharmaceuticals

☁️ SaaS

💰 Private Equity Round - WCG on 2019-11

Healthcare • Pharmaceuticals • SaaS

WCG is a global clinical research services and technology company that supports sponsors, CROs, research sites, and institutions across the lifecycle of clinical trials. Founded as a leader in independent ethical review, WCG provides IRB and IBC review, data monitoring committees, site enablement and study start-up services, participant recruitment and retention, and data & insights (including benchmarking, statistical consulting, and AI-powered trial foresight). The company also offers a suite of technology platforms (e. g. , ClinSphere®, eReview Manager, Total Enrollment, Total Feasibility) and large protocol and performance datasets to help design, plan, and run trials more efficiently and compliantly. WCG positions itself as a partner to biopharma and medical research organizations to accelerate trial activation, improve enrollment, and ensure regulatory and ethical compliance.

📋 Description

• 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

• 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

• 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