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bioMérieux

Global in vitro diagnostics for infectious diseases

Reimbursement Coding & Strategy Director

Biology & BiotechPosted on Nov 10
Full-timeUnited States

About the Job

Requirements

  • Bachelor's degree in Health Policy, Political Science, Life Sciences, Law, Public Health, Economics, or Business.
  • Seven or more years of healthcare experience in the clinical laboratory and/or biotechnology industries.
  • Three or more years of Medicare Policy experience.
  • Demonstrated knowledge and experience of the U.S. healthcare policy and market access landscape.
  • A proven track record in building relationships and advocating for policy changes.
  • Strong strategy, innovation, collaboration, and analytical skills.
  • Ability to lead delivery and creation of tailored communications to educate and mobilize critical stakeholders.
  • Deep understanding of the U.S. Market Access environment, including the U.S. payer system, coding, payment, coverage, and stakeholder engagement.
  • Ability to work independently and interdependently in cross-functional matrix teams.
  • Ability to prioritize multiple priorities, model leadership behaviors, and create partnerships across functions.
  • Highest standards of ethics and integrity.
  • Ability to remain in a stationary position, often standing, for prolonged periods.
  • Ability to ascend and descend stairs, ladders, ramps, and similar structures.
  • Legal authorization to work in the United States is required for new hires.

Responsibilities

  • Lead development of U.S. coding strategies for pipeline, launch, and on-market diagnostic products.
  • Assess available coding pathways, including CPT, PLA, HCPCS, and ICD-10 considerations, and recommend pathways supporting intended use, site of service, and reimbursement objectives.
  • Identify coding gaps, risks, dependencies, and decision points early in product development and translate findings into actionable recommendations for governance and product teams.
  • Develop long-range coding roadmaps covering milestones, evidence needs, submission timing, ownership, and contingency approaches.
  • Evaluate whether existing codes are appropriate or new or revised codes are needed, documenting rationale, business impact, and implementation considerations.
  • Adjust strategies for existing products in response to product changes, utilization patterns, coding updates, or reimbursement barriers.
  • Lead or coordinate preparation of coding applications, supporting narratives, technical documentation, and evidence packages with relevant internal subject-matter experts.
  • Define clinical, technical, utilization, and economic evidence needed to support coding objectives and incorporate requirements into evidence-generation plans.
  • Ensure coding submissions and supporting materials accurately reflect product characteristics, intended use, clinical utility, and applicable diagnostic pathways.
  • Maintain centralized records of coding decisions, assumptions, submission history, status, risks, and outcomes.
  • Coordinate internal review and approval of coding materials in accordance with company requirements and applicable standards.
  • Represent and attend AMA, ADLM, ACLA, CAP, and AMP.
  • Represent Market Access and coding strategy in U.S. go-to-market, pipeline, and lifecycle governance processes.
  • Integrate coding considerations into product profiles, evidence plans, launch sequencing, pricing and reimbursement planning, and commercial readiness activities.
  • Provide U.S. coding insights to global teams and adapt global market access tools to U.S. coding requirements.
  • Partner with brand and commercial teams to develop coding-related launch plans, customer resources, internal training, and objection-handling tools.
  • Assess operational implications of coding decisions for laboratories, providers, revenue cycle teams, sales teams, and customer support functions.
  • Monitor coding publications, code-set updates, application cycles, and industry developments affecting pipeline or on-market products.
  • Analyze potential business and access impact, communicate findings to stakeholders, and recommend response plans.
  • Establish coding governance tools, decision frameworks, standard operating practices, and performance measures.
  • Develop and maintain approved coding guides, reimbursement resources, training materials, and internal reference tools.
  • Serve as an internal expert and educator on diagnostic coding concepts, pathways, limitations, and appropriate use of coding information.
  • Collect field and customer insights about coding barriers and use them to refine product-level strategies and close access gaps.
  • Perform work in compliance with company quality procedures and standards.
  • Perform other duties as assigned.

Desired Qualifications

  • Diagnostic or medical device experience, including familiarity with laboratory diagnostic technologies, regulatory impacts, commercialization, and reimbursement considerations.
  • An advanced degree, such as an MBA or MPH.

About the Company

bioMérieux

Global in vitro diagnostics for infectious diseases

bioMérieux provides medical diagnostics worldwide by developing, manufacturing, and selling diagnostic tests, instruments, and software that detect infectious diseases and antimicrobial resistance. Its products work by analyzing patient samples through diagnostic assays and integrated systems that combine reagents, specialized instruments, and software to produce actionable test results for healthcare providers, laboratories, and public health agencies. The company stands out from competitors through its global leadership in in vitro diagnostics, a broad portfolio of instruments, reagents, and software, and a strong emphasis on public health and antimicrobial resistance challenges. Its goal is to improve patient care and public health by delivering timely, accurate diagnoses that help guide treatment and curb the spread of infectious diseases.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Marcy-l'Étoile, France
Founded
1963

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