Associate Medical Director, Gynecologic Oncology

Natera
United States
Workplace: RemoteFull timeUSD 188,500 - 235,600 annuallyFunction: Healthcare (Clinical, Medical, Wellness)Education: professionalSkills: ["Communication","Leadership","Project management","Cross-functional collaboration","Scientific storytelling"]

Lead clinical development and medical strategy for cfDNA/liquid biopsy in gynecologic oncology, focusing on MRD, recurrence monitoring, and clinical utility. Drive evidence generation, education, and cross-functional collaboration with R&D, commercial, and medical affairs to advance diagnostic solutions and oncology portfolio adoption.

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FursaFursa
Natera
Natera
3 months ago

Associate Medical Director, Gynecologic Oncology

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Last checked: 15 minutes agoStatus: Live

Job Summary

Lead clinical development and medical strategy for cfDNA/liquid biopsy in gynecologic oncology, focusing on MRD, recurrence monitoring, and clinical utility. Drive evidence generation, education, and cross-functional collaboration with R&D, commercial, and medical affairs to advance diagnostic solutions and oncology portfolio adoption.
Location: United States
Workplace: Remote
Employment Type: Full time
Job Function: Healthcare (Clinical, Medical, Wellness)

Key Responsibilities

  • •Partner with the Sr. Medical Director, Oncology on the 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 that demonstrate clinical utility in 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.
  • •Represent Natera at medical congresses and industry events, including SGO, ASCO, and ESMO, in person and virtually; build and maintain relationships with external experts and professional societies.
  • •Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development, endpoint selection, data analysis, publications, and congress submissions in gynecologic oncology.

Pay and Benefits

Salary: USD 188,500 - 235,600 annually
Equity and Bonus:Equity
Perks:Health Insurance401kPaid LeaveEquity

Key Requirements

  • •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.
  • •Ability to communicate credibly across solid tumor histologies and indications to support cross-portfolio initiatives.
  • •Excellent written and oral communication skills with strong presentation, scientific storytelling, and real-time problem-solving abilities.
Experience:OncologyClinical researchBiopharmaGynecologic oncology
Education:Professional (JD, MD, etc.)
Skills:CommunicationLeadershipProject managementCross-functional collaborationScientific storytelling
Languages:English
Tech Stack:Clinical researchBiostatisticsRegulatoryEndpoint designProtocol development

Company Brief

Natera
Develops and commercializes genetic testing and diagnostics focused on reproductive health, oncology, and organ transplant to inform clinical decision-making and improve patient outcomes.
Industry: Diagnostics
Company Size: Enterprise (1,001+ employees)
Revenue: USD 500M to 1B
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: San Carlos, United States
Founded: 2004
WebsiteLinkedIn