Provide medical and scientific leadership for Natera-sponsored oncology clinical trials focused on minimal residual disease (MRD).
Drive the design and execution of biomarker-driven interventional and randomized studies.
Serve as the program-level medical lead for Natera-sponsored MRD clinical trials across assigned oncology indications.
Define clinical development strategies and provide medical oversight across the full trial lifecycle.
Provide strategic and medical guidance to Clinical Scientists and act as Medical Monitor overseeing safety signal detection and risk mitigation.
Collaborate with cross-functional teams and partner with Regulatory Affairs to support submissions and responses.

MD (or equivalent).
≥3 years of industry experience in oncology clinical development.
Demonstrated experience serving as Medical Monitor or clinical lead for Phase II–III studies.
Strong working knowledge of GCP, ICH guidelines, and regulatory expectations for interventional trials.
Proven ability to interpret and communicate complex clinical data to internal and external stakeholders.

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

Clinical Director, Oncology Clinical Development

Key skills