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Head of Product Management

AccuScan SciencesMilpitas, California🇺🇸United StatesPosted 23 Jun 2026

Why This Role Stands Out

This leadership role offers a unique opportunity to shape the future of precision diagnostics in oncology, driving impactful product strategy within a reputable biotechnology company. If you have extensive product management experience in oncology diagnostics and a passion for translating scientific innovation into life-changing solutions, you'll thrive in this hybrid position. Apply now to lead product development and contribute to advancing cancer care globally.

Quick Overview

Seniority
Leader
Employment type
Full Time
Work mode
Hybrid
Location
Milpitas, California, United States
Posted
2 months ago

Job Description

AccuScan Sciences is a liquid biopsy biotechnology company developing whole-genome sequencing solutions for minimal residual disease detection in oncology. The team is focused on turning complex clinical and genomic insights into products that can support more informed cancer care and broaden the impact of precision diagnostics.

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.
  • 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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