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Staff Biostatistician (Analytical Validation)

External
natera logoNatera · Remote
$164K–$205K/yrFull-timeRemote1mo ago
ComplianceDocumentationLeadership
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Requirements

  • Minimum 8 years of relevant industry experience, with a focus on analytical validation in diagnostics, biotechnology, or related industries.
  • Ph.D. or Master's degree in Biostatistics, Statistics, or a related field.
  • KNOWLEDGE, SKILLS, AND ABILITIES:
  • Expert-level knowledge of statistical methodology in diagnostic medicine, including a deep understanding of CLSI guidelines
  • Exemplary written and verbal communication skills, with a specific talent for presenting to non-technical executive leadership
  • Demonstrated ability and enthusiasm for working on cross-functional teams with members of diverse technical backgrounds
  • Exceptional problem-solving skills and attention to detail
  • Remote USA
  • $164,000 - $205,000 USD
  • OUR OPPORTUNITY

Benefits

For more information, visit www.natera.com .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 intervieHealth insuranceDental insuranceVision insurance401(k)Remote work options

Additional Information

This is an exciting opportunity to independently lead Biostatistics efforts advancing Natera's oncology portfolio of cutting-edge molecular diagnostic tests. As a Staff Biostatistician, you will leverage your strong applied statistics expertise to drive the strategy and execution of complex validation experiments for multiple high-priority projects. The ideal candidate will possess exceptional communication skills and a deep understanding of Biostatistics in analytical validation. PRIMARY RESPONSIBILITIES: Strategic Study Design and Analysis : Independently lead the design, analysis, and interpretation of analytical validation studies for oncology products. Cross-Functional Leadership : Serve as the statistical lead on multiple high-priority project teams. Partner with bench scientists, bioinformatics, and product development teams to integrate statistical expertise into project planning and execution. Identify risks, communicate concerns, and champion solutions to interdisciplinary teams. Documentation and Reporting : Prepare comprehensive protocols and reports for cross-functional collaborators and stakeholders. Regulatory Compliance : Ensure statistical methodologies and analyses meet the standards set by regulatory agencies such as CAP/CLIA, NYS, and the FDA. Innovation and Improvement : Provide leadership on the application of both common and cutting-edge statistical methods for studies of varying complexity.

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