Natera

Director of Biostatistics (R&D)

Natera$193K — $242K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 8+ years in industry, 5+ years in diagnostics with a preference for NGS, genetics, and oncology experience.
  • 5+ years in a leadership role overseeing teams.
  • Master's in statistics, biostatistics, or similar; PhD preferred.
  • Robust knowledge of statistical methodologies in diagnostics, including FDA guidelines.
  • Experience working directly with regulatory bodies like the FDA.

Responsibilities

  • Lead and develop a high-performing biostatistics team and promote collaboration.
  • Oversee statistical study design and analysis for oncology product development.
  • Collaborate with cross-functional teams, integrating statistical expertise into project workflow.
  • Prepare protocols and reports for internal and external stakeholders.
  • Ensure compliance with regulatory standards and lead statistical discussions with regulatory agencies.
  • Innovate and apply advanced statistical methods for complex studies.
  • Drive team efficiency and quality of statistical analyses aligned with company goals.

Benefits

  • Opportunity to lead innovative statistical projects in oncology diagnostics.
  • Remote work flexibility offering work-life balance.
  • Fostering professional and technical development within the team.
  • Collaborative environment with cross-functional teams across the organization.
  • Role in shaping departmental standards and practices.
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.


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

$193,600-$242,000 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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