Senior Clinical Scientist, ECD

Natera; United States; Remote; USD 100,000 - 130,000; Full time

Benefits offered by this job

Comprehensive medical, dental, vision, life, and disability plans

Free testing and fertility care benefits

Pregnancy and baby bonding leave

401(k) benefits

Generous employee referral program

Job summary

Natera is looking for a Senior Clinical Scientist to lead clinical development for their early cancer detection program. This role involves overseeing study execution, clinical data review, and driving overall strategy. The ideal candidate should have over 6 years of experience and a strong background in clinical science.

Competitive benefits include comprehensive medical plans and generous leave policies.

Qualifications

• 6+ years of experience in clinical research, clinical science, or related field.
• Strong experience leading clinical studies and contributing to study design.
• Demonstrated experience in clinical data review and decision-making.

Responsibilities

• Lead execution of key components of clinical development for early cancer detection.
• Drive study design, including objectives and endpoints.
• Analyze complex datasets to identify trends and risks.

Skills

Clinical research

Data analysis

Cross-functional collaboration

Problem solving

Education

Advanced degree (PhD, PharmD, MD, or equivalent)

Job description

Senior Clinical Scientist

We are seeking a Senior Clinical Scientist to lead execution of key components of clinical development for our early cancer detection (ECD) program. This role is central to leading study execution, clinical data review, study design, and generation of scientific insights across multiple studies. The successful candidate will contribute meaningfully to clinical development strategy through hands‑on study leadership, cross‑functional execution, and data‑driven decision‑making.

You will serve as a clinical science lead within cross‑functional teams—partnering closely with Clinical Operations, Biostatistics, Medical Affairs, and Regulatory to drive study execution, identify risks and opportunities, and contribute to clinical development strategy through study‑level leadership and scientific insight.

This role is best suited for a clinical scientist who enjoys remaining closely involved in study execution, clinical data review, and cross‑functional problem solving while contributing to broader clinical development discussions and strategy.

Location: San Carlos, CA or Remote, USA (West Coast or Mountain time zones preferred)

Primary Responsibilities

Lead Clinical Development & Study Design

• 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
• Contribute to process improvements and development of best practices

Drive Data Review & Strategic Insight

• Lead medical and clinical data review to ensure data quality and integrity
• Analyze complex datasets to identify trends, risks, and opportunities
• Translate data into actionable insights that inform study and program decisions
• Partner with safety and medical teams on signal detection and escalation

Lead Cross‑Functional Execution

• Own day‑to‑day clinical science responsibilities across assigned studies
• Drive resolution of study‑level issues, risks, and operational challenges
• Partner closely with Clinical Operations, Medical Affairs, Regulatory, and Biostatistics to monitor study conduct, data quality, enrollment performance, and milestone delivery
• Make study‑level decisions and recommendations in ambiguous situations with limited oversight
• Represent Clinical Science in internal and external forums (e.g., investigators, KOLs)

Drive Study Performance & Program Value

• Prioritize activities across studies to ensure quality, timelines, and program impact
• Actively monitor study conduct, enrollment performance, protocol compliance, and clinical data quality across studies
• Identify operational risks early and implement corrective actions to maintain study timelines and quality

Advance Scientific Communication

• Lead development of abstracts, presentations, and manuscripts
• Translate clinical and statistical results into clear scientific narratives
• Support internal decision‑making and external evidence generation

Qualifications

• 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

Preferred Qualifications

• Experience in oncology, diagnostics, or early cancer detection
• Experience working across multiple studies or programs
• Track record of scientific publications and conference presentations

Knowledge, Skills, and Abilities

• Ability to lead complex clinical studies or multiple workstreams independently
• Ability to balance scientific rigor with pragmatic decision‑making in a fast‑paced environment
• Demonstrated ownership mindset with willingness to operate outside traditional functional boundaries when needed to advance study and program goals
• Strong analytical skills with ability to synthesize complex data into decisions
• Effective influencer across functions and senior stakeholders
• Excellent scientific communication skills

Benefits

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

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.