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Senior Staff Bioinformatics Scientist bei AccuraGen

AccuraGen · San Jose, Vereinigte Staaten Von Amerika · On-site

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Description

As a Senior Staff Bioinformatics Scientist at AccuScan Science, you will lead the development and improvement of statistical and algorithmic methods for NGS-based variant detection and minimal residual disease (MRD) calling. This role focuses on tumor/normal variant calling in tissue samples as well as ultra–low-frequency mutation detection in cfDNA.

You will work closely with assay development, bioinformatics engineering, and R&D teams to translate new technologies into robust, production-ready analytical pipelines. The ideal candidate brings deep statistical modeling expertise, strong hands-on implementation skills, and experience working with WGS or large-scale sequencing data. Prior exposure to regulated (FDA/IVD) environments and machine learning is a strong plus.

Key Responsibilities

  • Improve and extend somatic variant-calling algorithms for tumor tissue and cfDNA-based mutation detection
  • Develop, validate, and refine MRD-calling algorithms with an emphasis on sensitivity, specificity, and robustness
  • Design and implement benchmarking, evaluation, and quality control (QC) methodologies
  • Lead troubleshooting efforts, including root-cause analysis of analytical or pipeline failures, and drive corrective actions
  • Implement algorithms in production-quality code and collaborate with engineering teams to integrate methods into scalable pipelines and workflows
  • Partner with assay development teams on new technologies and assay iterations requiring customized analysis strategies and algorithm development
  • Document analytical methods, validation results, and design decisions; clearly communicate findings, limitations, and trade-offs to technical and cross-functional stakeholders

Requirements

  • Ph.D. in Statistics, Biostatistics, Computer Science, Bioinformatics, Computational Biology, Applied Mathematics, or a related field, with relevant postdoctoral or industry experience
  • Strong foundation in statistical inference and modeling, including uncertainty quantification and decision thresholding
  • Prior experience working with genomics data, including WGS or large-scale NGS datasets, and a solid understanding of technical and biological noise sources
  • Demonstrated software implementation skills in Python and/or a performance-oriented language (e.g., C++, Rust, Java), with experience writing maintainable, testable, production-quality code
  • Familiarity with standard genomics data formats and tooling (e.g., FASTQ, BAM/CRAM, VCF) and common processing workflows
  • Experience working in regulated product development environments (e.g., FDA, IVD), including documentation practices, analytical validation, and design controls
  • Excellent communication and collaboration skills, with the ability to work effectively across research, engineering, and assay development teams

Preferred Qualifications

  • Hands-on experience with cfDNA analysis and/or MRD detection, including ultra–low-frequency variant calling and/or epigenetics-based analyses
  • Machine learning experience, particularly in settings involving class imbalance, model evaluation, calibration, and decision optimization
  • Experience collaborating closely with assay development teams on experimental design, data analysis planning, and iterative assay optimization

Benefits

  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan (401k, IRA)
  • Paid Time Off (Vacation, Sick & Public Holidays)
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