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Natera

Makes genetic tests for clinical care

Staff Biostatistician - Clinical Validation

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeRemote in USA$164k - $205kRemote

About the Job

Requirements

  • Ph.D. or Master's degree in Biostatistics, Statistics, or a related field.
  • At least 8 years of relevant industry experience, preferably within molecular diagnostics, biotechnology, or related fields.
  • Demonstrated experience in regulated environments, including previous companion diagnostic or in vitro diagnostic submission experience.
  • Experience with next-generation sequencing, genetic, and/or germline-related data.
  • At least 4 years of practical experience with R statistical analysis software.
  • Expert working knowledge of statistical methodology in diagnostic medicine, including an understanding of Food and Drug Administration guidelines.
  • Previous experience interacting with regulatory bodies such as the Food and Drug Administration.
  • Experience designing and analyzing clinical validation studies.
  • Strong communication skills, including the ability to explain complex statistical concepts to non-statistical audiences.
  • Attention to detail and a commitment to delivering high-quality work under tight deadlines.

Responsibilities

  • Independently lead the design, analysis, and interpretation of clinical validation studies to support in vitro diagnostic approvals, such as companion diagnostics, 510(k), and premarket approval submissions.
  • Ensure statistical methodologies and analyses meet regulatory agency standards, including those of the Food and Drug Administration, and drive statistical interactions with regulatory authorities.
  • Prepare statistical analysis protocols, reports, and presentations for cross-functional and external collaborators and stakeholders.
  • Serve as the statistical lead on high-priority project teams; partner with Clinical Science, Data Management, and Product teams to integrate statistical expertise into project planning and execution; identify risks, communicate concerns, and champion solutions to interdisciplinary project teams.
  • Drive the design and execution of clinical research trials, studies, and publications to support product development.
  • Stay current with advances in biostatistics and clinical validation methodology and implement innovative approaches to support diagnostic product development and regulatory submissions.
  • Mentor and provide technical supervision to junior team members.

Desired Qualifications

  • Prior experience with germline assay development.
  • Prior experience with kidney disease.

About the Company

Natera

Makes genetic tests for clinical care

Natera develops genetic tests for clinicians caring for people with cancer, inherited conditions, pregnancies, and organ transplants, using DNA analysis to inform medical decisions. Its portfolio includes Signatera for tracking residual cancer, Panorama for prenatal screening, and Prospera for assessing transplanted organ health. The company combines laboratory analysis with software that distinguishes DNA fragments in blood, and earns revenue mainly from diagnostic testing, alongside licensing and services for research partners. Clinicians use its portals to order tests, track samples, and review results, while patients have access to genetic information sessions. Natera was founded in 2004 and is headquartered in Austin, Texas.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Austin, TX
Founded
2004

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