Principal Clinical Scientist

🕒 May 1

🇺🇸 United States – Remote

💵 $187.8k - $234.8k / year

⏰ Full Time

🔴 Lead

🧪 Clinical Research

🦅 H1B Visa Sponsor

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Logo of Natera

Natera

1001 - 5000 employees

Founded 2004

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

Biotechnology • Healthcare Insurance • Pharmaceuticals

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 MCED 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. • Partner with safety and medical teams on signal detection and escalation. • Lead cross-functional study teams and coordinate execution across functions. • Collaborate with Clinical Operations, Biostatistics, Medical Affairs, and Regulatory. • Represent Clinical Science in internal and external forums (e.g., investigators, KOLs). • Oversee enrollment, site performance, and key study metrics across studies. • Identify risks and proactively adjust study-level strategies. • Contribute to forecasting, planning, and milestone delivery. • Lead development of abstracts, presentations, and manuscripts. • Translate clinical and statistical results into clear scientific narratives.

🎯 Requirements

• Advanced degree (PhD, PharmD, MD, or equivalent; MS/RN with experience considered). • 8–12 years of experience in clinical research, clinical science, or related field. • Strong experience leading clinical studies and contributing to study design. • Experience with clinical data review and interpretation.

🏖️ Benefits

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

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