Staff Biostatistician (Clinical Validation)

Natera
San Carlos, CA

Who this role is best for

Geared toward candidates with regulated IVD experience comfortable with clinical validation study design and cross-functional leadership.

Best fit for

  • Candidates with 8+ years in molecular diagnostics and experience in FDA-regulated submissions
    — “At least 8 years of relevant industry experience, preferably within molecular diagnostics, biotechnology, or related fields.”
  • Individuals who have led clinical validation studies and can interpret complex statistical results
    — “Independently lead the design, analysis, and interpretation of clinical validation studies”
  • Professionals with strong documentation skills and a track record of preparing SAPs and reports
    — “Strong track record of producing high quality written documentation for multiple audiences”

Things to consider

  • The role demands a deep understanding of FDA guidelines and regulatory interactions
    — “Expert working knowledge of statistical methodology in diagnostic medicine, including an understanding of FDA guidelines”
  • Candidates must be prepared to work with germline and kidney disease data, which may be niche
    — “Prior experience with germline assay development preferred”

How to stand out

  • Highlight experience with NGS data and germline-related projects in your resume and interviews
    — “Experience with next-generation sequencing (NGS), genetic, and/or germline-related data.”
  • Emphasize your ability to communicate complex statistical concepts to non-statistical audiences
    — “Strong communication skills, with the ability to explain complex statistical concepts to non-statistical audiences.”
  • Demonstrate leadership in cross-functional teams through specific examples in your application materials
    — “Serve as the statistical lead on high-priority project teams. Partner with Clinical Science, Data Management, and Product teams”
Pace · SteadyCollaboration · MediumAutonomy · HighDecision Impact · Team

Derived from job-description analysis by Serendipath's career intelligence engine.

What success looks like

  • independent design, analysis, and interpretation of clinical validation studies
  • statistical interactions with regulatory authorities
  • comprehensive statistical analysis protocols (SAPs)
Typical background
Ph.D. or Master's degree in Biostatistics, Statistics, or a related field8+ years of relevant industry experience

Skills & requirements

Required

Applied StatisticsIVDClinical ResearchR Statistical Analysis SoftwareFDA Guidelines

Preferred

Next-generation Sequencing (ngs)GeneticGermline-related Data

Stack & domain

R Statistical Analysis SoftwareNext-generation Sequencing (ngs)GeneticGermline-related DataStatistical Analysis Protocols (saps)FDA GuidelinesCommunicationTeamworkLeadershipAttention To DetailBiostatisticsClinical ValidationRegulatory ComplianceStatistical Methodologies

About the role

Original posting from Natera via Greenhouse

This is an exciting opportunity to advance Natera’s regulated product portfolio of cutting-edge molecular diagnostic tests. As a Staff Biostatistician, you will leverage your strong applied statistics, IVD, and Clinical Research expertise to drive the strategy, design, analysis, and interpretation of clinical validation studies for kidney disease and other high-priority germline projects.

PRIMARY RESPONSIBILITIES: 

Strategic Study Design and Analysis: Independently lead the design, analysis, and interpretation of clinical validation studies to support in vitro diagnostic approvals (e.g., CDx, 510(k), PMA, etc.) 

Regulatory Compliance: Ensure statistical methodologies and analyses meet the standards set by regulatory agencies such as FDA. Drive statistical interactions with regulatory authorities.

Documentation and Reporting: Prepare comprehensive statistical analysis protocols (SAPs), reports, and presentations for cross-functional and external collaborators and stakeholders.

Cross-Functional Leadership: 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

Clinical Research and Beyond: Drive design and execution of high-impact research clinical trials, studies, and publications that push the development of our world-class product portfolio

Stay current with advancements in Biostatistics and clinical validation methodology, implementing innovative approaches to support diagnostic product development and regulatory submissions

Mentor and provide technical supervision to junior team members

QUALIFICATIONS: 

Education: Ph.D. or Master's degree in Biostatistics, Statistics, or a related field

Experience: 

At least 8 years of relevant industry experience, preferably within molecular diagnostics, biotechnology, or related fields.

Demonstrated experience in regulated environments, including previous CDx or IVD submission experience

Experience with next-generation sequencing (NGS), genetic, and/or germline-related data.

Minimum of 4 years practical experience with R statistical analysis software

KNOWLEDGE, SKILLS, AND ABILITIES: 

Expert working knowledge of statistical methodology in diagnostic medicine, including an understanding of FDA guidelines 

Previous experience interacting with regulatory bodies such as the FDA.

Demonstrated ability and enthusiasm for working on cross-functional teams with members of diverse technical backgrounds

Strong track record of producing high quality written documentation for multiple audiences 

Prior experience with germline assay development preferred

Prior experience with kidney disease desired

Experience in design and analyses of clinical validation studies

Strong communication skills, with 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.

Compensation & Total Rewards 

This range reflects a good-faith estimate of the base pay we reasonably expect to offer at the time of  hire. Final compensation will vary based on experience, qualifications, and internal equity considerations.

This position is also eligible for additional compensation and benefits through Natera’s robust Total Rewards program, including:

Annual performance incentive bonus

Long-term equity awards

Comprehensive health benefits (medical, dental, vision)

401(k) with company match

Generous paid time off and company holidays

Additional wellness and work-life benefits

Compensation Range $180,400—$225,500 USDOUR OPPORTUNITY

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

For more information, visit www.natera.com.

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.

If you are based in California, we encourage you to read this important information for California residents. 

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.

For more information:

  • BBB announcement on job scams 
  • FBI Cyber Crime resource page 

Source: Natera careers (Greenhouse)

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