Director of Product Management

AccuraGen

$130K — $180K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 8+ years of product management experience in oncology or molecular diagnostics.
  • Experience launching regulated IVD or LDT products globally.
  • Strong knowledge of MRD and liquid biopsy, plus clinical evidence strategy experience.
  • Familiarity with regulatory frameworks like MolDx, IVDR, and PMDA.
  • Effective communication with key opinion leaders and cross-functional teams is critical.
  • Must have eligibility to work in the United States.
  • A PhD or MBA is preferred but not mandatory.

Responsibilities

  • Define the product roadmap for MRD assays across various indications.
  • Translate clinical data into actionable product requirements and market claims.
  • Support strategies for regulatory compliance and reimbursement related to MolDx, IVDR, and PMDA.
  • Drive the development of global market strategy for oncology products.
  • Coordinate cross-functional execution throughout product development and launch phases.
  • Engage with key opinion leaders and partners to shape product direction.

Benefits

  • Comprehensive health and wellness programs.
  • Professional development opportunities.
  • Flexible work arrangements.
  • Collaborative and innovative work environment.
Full Job Description
In this role, you will shape product strategy for a growing oncology portfolio, helping connect scientific innovation, clinical evidence, and market needs. You will work across internal teams and external stakeholders to guide how products are defined, positioned, and advanced in regulated global markets.
Responsibilities
  • Define the product roadmap for MRD assays across multiple indications.
  • Translate clinical data into product requirements, claims, and market positioning.
  • Support regulatory and reimbursement strategies, including work related to MolDx, IVDR, and PMDA.
  • Drive global market strategy.
  • Coordinate cross-functional execution from development through launch.
  • Engage key opinion leaders, partners, and consortia to inform product direction.

Requirements
  • 8+ years of product management experience in oncology diagnostics or molecular diagnostics.
  • Experience launching regulated IVD or LDT products across global markets.
  • Strong knowledge of MRD and liquid biopsy, with experience in clinical evidence strategy.
  • Experience working with MolDx, IVDR, and PMDA.
  • Proven ability to interface effectively with key opinion leaders, commercial leadership, regulatory teams, reimbursement teams, and external partners.
  • Must be eligible to work in the United States.
  • A PhD or MBA is a plus.

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