Назад
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12 дней назад

Sr. Medicare Coverage Analyst

77 500 - 90 400$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Sr. Medicare Coverage Analyst (Medicare/Clinical Trials): Reviewing clinical research protocols and related documents to create coverage analyses and billing guides with an accent on Medicare policy, billing compliance, and clinical trial workflows. Focus on assessing qualifying clinical trials, resolving complex coverage determinations, prioritizing urgent amendments, and mentoring junior analysts.

Location: Boston, Massachusetts, United States; 100% remote

Salary: $77,500–$90,400 per year

Company

hirify.global conducts cancer research, provides patient care, educates medical researchers, and advances public health programs.

What you will do

  • Review clinical research protocols, informed consent forms, clinical trial agreements, and related study documents.
  • Create coverage analysis grids and billing guides for complex clinical research protocols.
  • Determine whether studies qualify under the Medicare Clinical Trial Policy and designate services billable to insurance or study sponsors.
  • Act as a subject matter expert on Medicare National and Local Coverage Determinations and communicate policy updates.
  • Prioritize coverage-analysis workflows and urgent protocol amendments while coordinating timelines with study teams and external stakeholders.
  • Resolve protocol assessment discrepancies with sponsors and advise study teams and principal investigators before submission.

Requirements

  • Bachelor’s degree or RN credential.
  • At least five years of Medicare coverage analysis experience.
  • Experience with research activities in an academic medical center.
  • Knowledge of billing compliance, Medicare regulations, applicable laws, and institutional procedures.
  • Knowledge of clinical research budgeting, the clinical trial lifecycle, and clinical trial management systems.
  • Ability to independently facilitate communication between study teams and sponsors.

Nice to have

  • CPT and DRG coding experience.
  • Experience mentoring or training junior staff.

Culture & Benefits

  • Fully remote work arrangement.
  • Inclusive, diverse, and equitable environment.
  • Work focused on cancer research, patient care, and public health.
  • Collaboration with Harvard Medical School-affiliated hospitals and other research partners.

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