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Natera

Staff Biostatistician (Clinical Validation)

Natera is hiring a Staff Biostatistician (Clinical Validation) for a remote role open to applicants in United States. Level rates it ; you can apply on Natera.

Level's read on this job

  • On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
  • The posting lists this role as remote.
  • Tools and skills the posting cites include R, biostatistics and clinical research.
  • Level lists 228 other open roles at Natera.
  • The role was posted within the past two weeks.

AI in this role

Staff Biostatistician to lead clinical validation studies and regulatory submissions for molecular diagnostic products.

r
biostatisticsclinical-researchregulatory-complianceivd

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.
The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.Remote USA$164,000—$205,000 USD

OUR 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 

How we rate this

Staff Biostatistician (Clinical Validation) at Natera rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

BiostatisticsClinical ResearchRegulatory ComplianceIvdR

Questions you could be asked

  1. Tell me about a project where biostatistics was part of your work. What did you do?
  2. Tell me about a project where clinical research was part of your work. What did you do?
  3. Tell me about a project where regulatory compliance was part of your work. What did you do?
  4. Tell me about a project where ivd was part of your work. What did you do?
  5. Walk me through how you've used R in your day-to-day work.

Adapt your resume

  • List these exact terms on your resume: Biostatistics, Clinical Research, Regulatory Compliance, Ivd, and R. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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