Senior Clinical Scientist, ECD

🕒 July 30

🏄 California – Remote

🏄 California – Remote

💵 $142.8k - $178.5k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 6%

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

• Lead substantial aspects of ECD clinical studies or multiple studies • Drive study design, including objectives, endpoints, eligibility criteria, and schedules of assessments • Author and review protocols, ICFs, CRFs, and study documents • Contribute meaningfully to clinical development strategy and study-level decision-making • Lead medical and clinical data review to ensure data quality and integrity • Analyze complex datasets to identify trends, risks, and opportunities • Own day-to-day clinical science responsibilities across assigned studies • Drive resolution of study-level issues, risks, and operational challenges • Prioritize activities across studies to ensure quality, timelines, and program impact • Lead development of abstracts, presentations, and manuscripts

🎯 Requirements

• Advanced degree (PhD, PharmD, MD, or equivalent; MS, MPH, RN with experience considered) • 6+ years of experience in clinical research, clinical science, or related field • Strong experience leading clinical studies and contributing to study design • Demonstrated experience leading and executing clinical studies, including clinical data review, study-level decision making, issue management, and cross-functional coordination

🏖️ Benefits

• Comprehensive medical, dental, vision, life and disability plans • Free testing for employees and their immediate families • Fertility care benefits • Pregnancy and baby bonding leave • 401k benefits • Commuter benefits • Employee referral program