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Associate Medical Director, Gynecologic Oncology

Natera· Medical Affairs - Oncology
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Remote$188.5k - $235.6kfull-timePosted 4mo ago

About the role

Clinical leadership role directing medical strategy and clinical development for cfDNA and liquid biopsy in gynecologic oncology, with focus on MRD and recurrence monitoring across ovarian, endometrial, cervical, vulvar, and vaginal cancers.

Responsibilities

  • Partner with the Sr. Medical Director, Oncology on clinical development of cfDNA molecular diagnostics and liquid biopsy assays for gynecologic cancers.
  • Direct the development and execution of clinical strategies and evidence-generation plans for gynecologic oncology, including 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 data-driven clinical evidence and educational materials to gynecologic oncology stakeholders.
  • Represent Natera at medical congresses and industry events (SGO, ASCO, ESMO) in person and virtually.
  • Build and maintain relationships with external experts, clinical investigators, cooperative groups (NRG/GOG), and professional societies in gynecologic oncology.
  • Maintain scientific rigor and data-driven urgency across the oncology organization.
  • Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development, endpoint selection, data analysis, interpretation, publications, and congress submissions.
  • Support investigator-initiated research, real-world evidence generation, and clinical collaborations to advance standard of care in gynecologic cancers.

Qualifications

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

Skills

Required:Gynecologic oncology expertiseMedical communication and educationCross-functional collaboration

Benefits

  • 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
Last updated Jul 9, 2026. Interested? Apply on the company site.

About Natera

A global leader in cfDNA testing

Dedicated to oncology, women’s health, and organ health. Natera’s cell-free DNA tests help protect health and inform more personalized decisions about care.

oncologywomen's healthorgan healthcell-free DNA
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