Natera

Director of Biostatistics (R&D)

Natera$213K — $267K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Minimum of 8 years of industry experience, including 5 years in diagnostics, preferably NGS, genetics, and oncology.
  • At least 5 years of team leadership experience.
  • Master's degree in statistics, biostatistics, or equivalent; PhD preferred.

Responsibilities

  • Build and mentor a high-performing biostatistics team, fostering collaboration.
  • Oversee design, statistical analysis, and interpretation of analytical validation studies.
  • Collaborate with scientists and regulatory teams to integrate statistical expertise into projects.
  • Prepare detailed protocols and reports for internal and external stakeholders.
  • Ensure compliance with CAP/CLIA and FDA standards in statistical methods and analyses.
  • Lead innovation in applying common and advanced statistical methods for studies.
  • Enhance team efficiency through innovative techniques and promote departmental standards.

Benefits

  • 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
Full Job Description
This is an exciting opportunity to lead a team of statisticians advancing Natera's oncology portfolio of cutting-edge molecular tests. As a Director, you will leverage your applied statistics expertise to the design, analysis, and interpretation of analytical validation studies, ensuring compliance with regulatory guidelines and driving data-informed decision-making. The ideal candidate will possess strong leadership and communication skills, and a deep understanding of biostatistics in analytical validation.

PRIMARY RESPONSIBILITIES:
  • Team Leadership: Build, mentor, and direct a high-performing biostatistics team, fostering collaboration, and overseeing their technical and professional development.
  • Study Design and Analysis: Oversee the design, statistical analysis, and interpretation of analytical validation studies in support of oncology product development.
  • Cross-Functional Collaboration: Partner with bench scientists, regulatory, 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 high-quality protocols and reports for cross-functional internal and external collaborators and stakeholders.
  • Regulatory Compliance: Ensure statistical methodologies and analyses meet the standards set by regulatory agencies such as CAP/CLIA and the FDA. Lead statistical interactions with regulatory agencies.
  • Innovation and Improvement: Provide leadership on the application of both common and cutting-edge statistical methods for studies of varying complexity.
  • Strategic Leadership: Continuously improve the efficiency and efficacy of the team through innovative techniques and strategies. Promote departmental standards for the development and execution of statistical analyses, ensuring alignment with company goals and regulatory requirements.

QUALIFICATIONS:
  • Minimum of 8 years of industry experience, including at least 5 years experience in diagnostics. Experience with NGS, genetics, and oncology preferred.
  • At least 5 years experience leading a team.
  • Master's degree in statistics, biostatistics, or equivalent, PhD preferred.

KNOWLEDGE, SKILLS, AND ABILITIES:
  • Aptitude for technical leadership and strategic thinking
  • Proven record of leading a successful team
  • Expert working knowledge of statistical methodology in diagnostic devices, including FDA guidelines.
  • 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 directly interacting with regulatory agencies such as FDA.


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

$213,800-$267,300 USD

About Natera

Natera is a biotechnology company that focuses on genetic testing and diagnostics. The company's products are designed to help diagnose and treat genetic diseases, cancer, and other conditions. Natera's pipeline includes products for reproductive health, oncology, and organ transplantation. The company was founded in 2003 and is headquartered in San Carlos, California.
Learn more about Natera
Size
2,670 employees
Market Cap
$4.5 billion
Industry
Net Income
-$229.7 million
Founded
2004
5 Year Trend
+24.1%
Revenue
$391 million
NASDAQ

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