Senior Clinical Scientist, ECD

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

Experience in oncology, diagnostics, or early cancer detection

Ability to lead complex clinical studies or multiple workstreams independently

Effective influencer across functions and senior stakeholders

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

For more information, visit

www.natera.com

.

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.

We are seeking a Principal Clinical Scientist to lead execution of key components of clinical development for our multi-cancer early detection (MCED) program.

This role is central to driving study design, clinical data review, and scientific insights across multiple studies.

You will serve as a clinical science lead within cross-functional teams – partnering with Clinical Operations, Biostatistics, Medical Affairs, and Regulatory to advance study execution and shape clinical strategy.

Lead Clinical Development & Study Design

Lead substantial aspects of MCED clinical studies or multiple studies

Drive study design, including objectives, endpoints, eligibility criteria, and schedules of assessments