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Natera

Lead Biostatistician (IVD Clinical)

RemoteUnited States only
Published
Role
Data Science
Experience
Lead
$130.9k–$163.6k/yr
Check eligibility

Open to US only. Set where you work from to check your eligibility.

No BS summary

Lead biostatistician for US remote work with 5+ years relevant experience with a master’s or 3+ years with a PhD. Must have regulated clinical-trial statistics experience for regulatory submissions and 4+ years with statistical analysis software such as R, SAS, or JMP. IVD/diagnostics, oncology, NGS/genetics, and FDA interaction are preferred.

Core skills

R/SAS/JMPBiostatistics

Optional skills

Next-generation sequencing

What you'll do

  • Design and review statistical methodology in protocols and statistical analysis plans
  • Lead execution of statistical analyses according to plans and protocols, as well as exploratory or ad-hoc analyses
  • Produce high quality presentations and author documentation of analysis plans, methods, results, and interpretation
  • Effectively convey statistical concepts and results to cross-functional internal and external collaborators and stakeholders
  • Identify risks, communicate concerns, and champion solutions to interdisciplinary project teams
  • Mentor and provide technical supervision to junior team members
  • Perform other duties as assigned

What they require

  • Master’s degree in biostatistics, statistics, or equivalent with 5+ years of relevant experience, or PhD in biostatistics, statistics, or equivalent with 3+ years of relevant experience
  • At least 3 years practical experience designing and executing statistical analyses in a regulated environment and clinical trials for regulatory submissions
  • Minimum of 4 years practical experience with statistical analysis software such as R (preferred), SAS, or JMP
  • Preferred: Previous diagnostic experience
  • Expert knowledge of probability theory and statistics including the ability to evaluate and produce novel methods and applications
  • Familiarity with typical approaches, best practices, and regulatory standards in clinical trial design
  • Demonstrated ability and enthusiasm for working on cross-functional teams with members of diverse technical backgrounds
  • Strong communication skills, with the ability to explain complex statistical concepts to non-statistical audiences
  • Track record of producing high quality written documentation for multiple audiences
  • Preferred: Prior experience with next-generation sequencing (NGS), genetics, and/or oncology testing
  • Preferred: Previous experience interacting with regulatory bodies such as the FDA

Benefits

  • Competitive Benefits
  • Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents
  • Natera employees and their immediate families receive free testing in addition to fertility care benefits
  • Pregnancy and baby bonding leave
  • 401k benefits
  • Commuter benefits
  • Generous employee referral program

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Its aim is to make personalized genetic testing and diagnostics part of the standard of care.

🇺🇸 United StatesHealthcareEnterprisenatera.com

What people say about this company

2.7/ 5

$130.9k–$163.6k/yr