Senior Clinical Scientist, ECD

POSITION SUMMARY:

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

The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.

Remote USA

$142,800 $178,500 USD

OUR OPPORTUNITY

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team cons…