Remote Senior Bioinformatics Manager, Clinical Genomics

Illumina, Inc.

San Diego (CA)

Remote

USD 171,000 - 256,000

Full time

14 days+

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Job summary

Illumina, Inc. is seeking a Sr. Manager, Bioinformatics to lead a team supporting Clinical Genomics across oncology, reproductive health, and regulated sequencing products.

You will oversee development, validation, and deployment of bioinformatics workflows enabling customer-facing software and regulatory submissions. You will partner with cross-functional teams to advance product capabilities, drive adoption with customers, and ensure high-quality scientific outcomes in a fast-paced, compliant

Qualifications

  • Bachelor’s degree with 12+ years of related experience, including 3–6 years in management.
  • PhD in Bioinformatics, Computational Biology, CS, Statistics, Genomics, or related field with 8+ years relevant experience preferred.
  • Demonstrated leadership in managing bioinformatics teams and cross-functional programs.

Responsibilities

  • Lead and mentor a team of bioinformatics scientists.
  • Oversee bioinformatics activities supporting Clinical Genomics product development, commercialization, and lifecycle management.
  • Develop, validate, and deploy analytical methods and bioinformatics workflows for customer-facing software and regulated products.
  • Collaborate with R&D, Software, Biostatistics, Regulatory, Quality, Product Management, and Commercial teams.
  • Partner with customers and external collaborators to support product adoption and gather feedback.

Skills

Leadership
Bioinformatics
Regulatory knowledge
Python
R
Linux
Collaboration
Communication
Biostatistics

Education

Bachelor's degree
PhD in related field

Tools

Git
Docker

Job description

Illumina, Inc. is seeking a Sr. Manager, Bioinformatics to lead a team supporting Clinical Genomics across oncology, reproductive health, and regulated sequencing products.

You will oversee development, validation, and deployment of bioinformatics workflows enabling customer-facing software and regulatory submissions. You will partner with cross-functional teams to advance product capabilities, drive adoption with customers, and ensure high-quality scientific outcomes in a fast-paced, compliant

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