Senior Research Associate

Natera
United States
Workplace: OnsiteFull timeUSD 108,600 - 135,700 annuallyFunction: Research & Scientific (R&D)Experience: 4+ yearsEducation: bachelorsSkills: ["Communication","Organizational skills","Record-keeping","Planning","Attention to detail"]

Develop and validate automated high-throughput NGS assays for FDA-submission and regulatory use as part of the Early Cancer Detection product development team. Design and execute verification and moderate-to-high complexity experiments, perform data analysis, and collaborate with assay development scientists, clinical lab, QA, automation engineering, bioinformatics, and statistics to ensure design-control compliance and high-quality clinical assay launches in a CLIA laboratory.

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FursaFursa
Natera
Natera
1 day ago

Senior Research Associate

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Source: Company careers pageValidated by: Fursa AI
Last checked: 1 hour agoStatus: Live
Reposted: similar role first listed 3 months ago

Job Summary

Develop and validate automated high-throughput NGS assays for FDA-submission and regulatory use as part of the Early Cancer Detection product development team. Design and execute verification and moderate-to-high complexity experiments, perform data analysis, and collaborate with assay development scientists, clinical lab, QA, automation engineering, bioinformatics, and statistics to ensure design-control compliance and high-quality clinical assay launches in a CLIA laboratory.
Location: United States
Workplace: Onsite
Employment Type: Full time
Job Function: Research & Scientific (R&D)
Seniority: Mid level

Key Responsibilities

  • •Design, develop, and validate automated high-throughput NGS assays for submission to FDA and regulatory bodies, run in a commercial single-site IVD CLIA laboratory.
  • •Implement NGS-based assay technical projects, including timelines and deliverables, and conduct moderate-to-high complexity experiments with basic data analysis.
  • •Coordinate assay specifications with assay development scientists for future production assays and collaborate with Clinical Laboratory and Quality Assurance to meet quality standards.
  • •Serve as point person across internal groups (automation engineering, laboratory operations, bioinformatics, statistics, project and product management) to ensure timely project execution and identify continuous improvements to shorten TAT.
  • •Write protocols, reports, and SOPs; train lab operations clinical lab scientists; and plan and execute verification activities.

Pay and Benefits

Salary: USD 108,600 - 135,700 annually
Perks:Health InsuranceDentalVision401kPaid Leave

Key Requirements

  • •Bachelor’s degree in molecular biology, genetics, biochemistry, cell biology, or related field with 4+ years relevant industry experience, or an M.S. with 2+ years in research/assay development.
  • •Experience with IVD product development and design controls.
  • •Strong understanding of nucleic acid extraction chemistry, PCR, NGS library preparation, and hybrid capture technologies.
  • •Hands-on experience preparing reagents and performing QC for NGS-based assays, including stability, guard banding, reproducibility, and repeatability studies.
  • •Experience working in a regulated laboratory environment under CLIA/CAP and performing data analysis (JMP and Excel).
Experience:4+ yearsIVDOncologyNGSRegulated laboratory
Education:Bachelor's
Skills:CommunicationOrganizational skillsRecord-keepingPlanningAttention to detail
Tech Stack:NGSPCRHybrid captureJMPExcelPythonRLiquid handler robotsCLIACAPLIMSAutomation

Company Brief

Natera
Develops and commercializes genetic testing and diagnostics focused on reproductive health, oncology, and organ transplant to inform clinical decision-making and improve patient outcomes.
Industry: Diagnostics
Company Size: Enterprise (1,001+ employees)
Revenue: USD 500M to 1B
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: San Carlos, United States
Founded: 2004
WebsiteLinkedIn