Lead Biostatistician, IVD Clinical

🕒 July 9

🇺🇸 United States – Remote

💵 $130.9k - $163.6k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 14%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Natera

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2004

🏥 Healthcare

🧬 Biotechnology

⚕️ Healthcare Insurance

Healthcare • Biotechnology • Healthcare Insurance

Natera is a global leader in cell-free DNA testing technology, specializing in non-invasive genetic testing and diagnostics. The company's innovative solutions focus on areas such as prenatal screening, cancer detection, and organ transplant monitoring. By using advanced bioinformatics and DNA analysis, Natera provides healthcare professionals and patients with critical information to make more informed medical decisions.

📋 Description

• 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.

🎯 Requirements

• 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. • Previous diagnostic experience preferred.

🏖️ Benefits

• Comprehensive medical, dental, vision, life and disability plans for eligible employees and dependents. • Free testing for employees and their immediate families. • Fertility care benefits. • Pregnancy and baby bonding leave. • 401(k) benefits. • Commuter benefits. • Generous employee referral program.