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Project Manager, NGS Clinical Diagnostics

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Summary

Project Manager leading NGS-based clinical diagnostics (LDTs) from concept through clinical launch at a Fremont, CA genomics company. Coordinates cross-functional teams across assay development, bioinformatics, lab operations, quality, and regulatory, with a focus on NGS workflows and CLIA/CAP compliance.

About the Role

We are seeking an experienced Project Manager to lead the development, validation, and commercialization of Next Generation Sequencing (NGS)-based Laboratory Developed Tests (LDTs). This role will coordinate cross-functional teams spanning assay development, bioinformatics, laboratory operations, quality, regulatory, and commercial functions to successfully launch new clinical testing services.

The ideal candidate combines strong project management skills with a solid understanding of NGS technologies and molecular diagnostics, enabling them to effectively drive technical programs from concept through clinical launch.


Key Responsibilities

Program Leadership

  • Develop and manage integrated project plans, timelines, milestones, and deliverables.
  • Lead cross-functional project teams and drive accountability across stakeholders.
  • Identify project risks, dependencies, and mitigation strategies.
  • Provide regular status updates to leadership and key stakeholders.

NGS and Technical Coordination

  • Coordinate development of NGS-based clinical assays from design through launch.
  • Work closely with scientists, bioinformaticians, and laboratory personnel to ensure successful execution of technical objectives.
  • Understand and track key assay performance metrics, validation requirements, and operational readiness activities.
  • Translate complex technical topics into clear project plans and business updates.

Validation and Clinical Launch

  • Coordinate analytical and clinical validation studies.
  • Ensure alignment of assay development, bioinformatics, quality, and regulatory activities.
  • Drive completion of documentation, SOPs, training, and launch-readiness requirements.
  • Support implementation of new tests into clinical laboratory operations.

Quality and Regulatory Collaboration

  • Partner with Quality and Regulatory teams to support CLIA, CAP, HIPAA, and applicable state compliance requirements.
  • Track validation documentation, change controls, audit readiness, and quality milestones.
  • Ensure compliance requirements are incorporated into project timelines and deliverables.

Commercial and Operational Readiness

  • Coordinate launch activities across operations, business development, marketing, and customer support teams.
  • Support laboratory capacity planning, customer onboarding, and implementation activities.
  • Facilitate communication between technical and commercial stakeholders to ensure successful market adoption.


Qualifications

Required

  • BS or MS in Molecular Biology, Genetics, Genomics, Bioinformatics, Biotechnology, Clinical Laboratory Science, or a related field.
  • 5+ years of project or program management experience in molecular diagnostics, genomics, biotechnology, or clinical laboratory environments.
  • Working knowledge of Next Generation Sequencing workflows, including sample preparation, sequencing, bioinformatics analysis, and clinical reporting.
  • Experience leading cross-functional technical projects.
  • Strong communication, organizational, and stakeholder management skills.

Preferred

  • Experience launching NGS-based clinical assays or LDTs.
  • Familiarity with CLIA and CAP laboratory environments.
  • Experience working with Illumina, PacBio, or Oxford Nanopore platforms.
  • PMP certification.
  • Knowledge of bioinformatics pipelines, variant interpretation, and genomic reporting workflows.

Skills

Apply

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