Associate Medical Director, Gynecologic Oncology

Natera

Associate Medical Director overseeing clinical development in gynecologic oncology for Natera's cfDNA portfolio. Collaborating across teams for molecular testing solutions and clinical education.

Posted 6/17/2026full-timeRemote • 🇺🇸 United StatesLead💰 $188,500 - $235,600 per yearWebsite

About the role

Key responsibilities & impact

Partner with the Sr. Medical Director, Oncology on the clinical development of cell-free DNA (cfDNA) molecular diagnostics and liquid biopsy assays for gynecologic cancers
Direct the development and execution of clinical strategies and evidence-generation plans that demonstrate clinical utility in gynecologic oncology, including minimal residual disease (MRD) tracking, recurrence monitoring, treatment response assessment, and clinical trial enrichment
Oversee medical education and scientific communications for healthcare providers focused on gynecologic oncology, including tumor boards, webinars, and field medical enablement
Partner with commercial and marketing teams to deliver clear, data-driven clinical evidence and educational materials to gynecologic oncology stakeholders
Represent Natera at medical congresses and industry events, including SGO, ASCO, and ESMO, both in person and virtually
Build and maintain relationships with external experts, clinical investigators, cooperative groups such as NRG/GOG, and professional societies within gynecologic oncology
Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development, endpoint selection, data analysis, data interpretation, peer-reviewed publications, and congress submissions in gynecologic oncology

Requirements

What you’ll need

M.D. or D.O. with board certification in Gynecologic Oncology, or Medical Oncology with a significant gynecologic oncology focus
Minimum 5 years of post-training experience in oncology with a strong background in clinical research and development; clinical diagnostics or biopharma industry experience is preferred
At least 3 years of clinical trial experience in academia, biopharma, biotech, diagnostics, or an equivalent clinical research setting
Title and level (Associate Medical Director or Medical Director) will be commensurate with experience

Benefits

Comp & perks

Annual performance incentive bonus
Long-term equity awards
Comprehensive health benefits (medical, dental, vision)
401(k) with company match
Generous paid time off and company holidays
Additional wellness and work-life benefits

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical developmentmolecular diagnosticsliquid biopsy assaysclinical strategiesevidence-generation plansclinical trial experiencedata analysisdata interpretationpeer-reviewed publicationsendpoint selection

Soft Skills

relationship buildingcollaborationcommunicationleadershipeducational material developmentscientific communicationdata-driven decision makingmedical educationstakeholder engagementpresentation skills

Certifications

M.D.D.O.board certification in Gynecologic Oncologyboard certification in Medical Oncology