Natera jobs

Natera is hiring a Clinical Oncology Specialist (COS) for breast oncology in the Keystone region (Eastern Shore, New Jersey, Philadelphia). The role focuses on promoting and driving adoption of Signatera, an MRD ctDNA test, among key opinion leaders including breast surgeons, radiologists, oncologists, and pathologists. Responsibilities include territory planning, account development, clinical education delivery, and sales activities. The position requires ~75% travel (road and air) with a preference for Philadelphia-based candidates and no remote option indicated.

Natera is hiring a Clinical Oncology Specialist (COS) for breast oncology in the Lake Effect region (Pittsburgh, Allentown, and West Virginia). The role focuses on promoting and driving adoption of Signatera, an MRD ctDNA test, among key opinion leaders including breast surgeons, radiologists, oncologists, and pathologists. Responsibilities include territory planning, account development, clinical education delivery, and sales activities. The position requires ~75% travel (road and air) with no remote option indicated.

Natera is hiring a Clinical Oncology Specialist (COS) for breast oncology in the Mid-Atlantic region (Baltimore, MD and Washington D.C.). The role focuses on promoting and driving adoption of Signatera, an MRD ctDNA test, among key opinion leaders including breast surgeons, radiologists, oncologists, and pathologists. Responsibilities include territory planning, account development, clinical education delivery, and sales activities. The position requires ~75% travel (road and air) with no remote option indicated.

Clinical Oncology Specialist for Natera's Breast Oncology team, covering North Central US (Iowa, Kansas, Missouri, Wisconsin, Dakotas). Focus on promoting Signatera MRD test to oncologists, surgeons, and radiologists. Requires 5+ years breast oncology/surgical sales or molecular diagnostics experience, 75% travel (road and air), valid driver's license. Territory-based medical device sales role.

Clinical Oncology Specialist, Breast Oncology at Natera is a medical device/diagnostic sales role focused on promoting the Signatera MRD test to oncologists and healthcare systems in the Gulf region (AL, TN, LA). Requires 5+ years breast oncology or surgical sales experience, frequent travel (~75%), and clinical acumen; on-site territory-based role.

Natera seeks a Clinical Oncology Specialist, Breast Oncology, to drive adoption of Signatera (MRD ctDNA test) among breast surgeons, oncologists, and other KOLs across integrated delivery networks and cancer centers in Northern Texas. The role requires 5+ years oncology/surgical/diagnostics sales experience, frequent travel (75%), and deep clinical knowledge of breast oncology.

Clinical Oncology Specialist, Breast Oncology at Natera in Northern California (Sacramento/San Francisco/San Jose area). Specialty sales role focused on promoting Signatera MRD ctDNA test to breast surgeons, oncologists, and radiologists. Responsibilities include territory planning, KOL engagement, clinical education, and adoption driving. Requires 5+ years breast oncology/surgical sales; ~75% travel. This is a specialized medical device sales role, not software engineering.

Clinical Oncology Specialist, Breast Oncology at Natera, a precision diagnostics company. The role is a field sales position focused on driving adoption of Signatera (MRD ctDNA test) among breast oncologists and surgeons across Arizona, Colorado, and New Mexico. Primary responsibilities include KOL engagement, clinical education, territory management, and account expansion. Requires 5+ years in breast oncology or molecular diagnostics sales, frequent travel (~75%), and valid driver's license.

Natera seeks a Manager, Clinical Lab to oversee lab workflow, production goals, quality assurance, and team performance in a diagnostic testing environment. Responsibilities include metrics monitoring, process improvement, compliance oversight, employee management, and troubleshooting lab errors. Based in San Carlos, CA on-site; requires lab operations management experience and regulatory compliance knowledge in clinical testing.