Associate Medical Director, Gynecologic Oncology

About the role

This leadership position will guide the medical strategy and clinical advancement of Natera's cell-free DNA and liquid biopsy offerings. You will focus on minimal residual disease detection and recurrence monitoring for women's cancers. Your work will involve close collaboration with various internal departments to ensure the scientific integrity and clinical value of our diagnostic tests.

Key facts

What you'll do

• Contribute to the clinical development of molecular diagnostics for gynecologic cancers, supporting the Senior Medical Director.
• Shape and implement clinical strategies to demonstrate the utility of our tests for tracking minimal residual disease, monitoring recurrence, assessing treatment response, and aiding in clinical trial selection.
• Oversee medical education initiatives and scientific communications for healthcare professionals in gynecologic oncology, including presentations and field support.
• Work with commercial and marketing teams to create clear, evidence-based educational materials for gynecologic oncology specialists.
• Represent Natera at key medical conferences and industry gatherings, both virtually and in person.
• Cultivate relationships with external medical experts, researchers, and professional organizations in the field.
• Collaborate with research, development, biostatistics, and clinical operations teams on study design, data analysis, publications, and presentations.
• Support investigator-initiated studies and real-world evidence generation to advance the standard of care.

Requirements

• Medical Doctor (MD) or Doctor of Osteopathic Medicine (DO) degree.
• Board certification in Gynecologic Oncology, or Medical Oncology with a substantial focus on gynecologic oncology.
• A minimum of 5 years of post-training experience in oncology, with a strong foundation in clinical research and development.
• At least 3 years of experience with clinical trials in an academic, biopharmaceutical, biotechnology, diagnostics, or similar research setting.
• Demonstrated ability to lead or participate in cross-functional teams, taking ownership and making decisions in a dynamic environment.
• Excellent written and verbal communication skills, with proficiency in scientific storytelling and problem-solving.
• Strong project management and organizational skills, with the capacity to manage multiple priorities under pressure.
• Experience working effectively across different departments and resolving challenges.
• Familiarity with clinical trial methodologies, protocol development, regulatory frameworks, statistics, and epidemiology.

Nice to have

• Prior experience in the clinical diagnostics or biopharmaceutical industry.
• Experience in developing and executing evidence generation plans for molecular diagnostics.

Skills & tools

• Deep understanding of gynecologic cancers, including treatment approaches, molecular markers (e.g., HRD, MSI/Lynch, HPV), and current clinical guidelines.
• Ability to communicate effectively with clinical audiences and payers regarding scientific data and clinical utility.
• Proficiency in understanding and communicating across various solid tumor types.
• Ability to quickly learn and articulate Natera's technologies and market position.

Practical notes

• Compensation range: $188,500 - $235,600 USD annually, plus annual performance bonus and long-term equity awards.
• Comprehensive benefits package including medical, dental, vision, 401(k) with company match, and generous paid time off.
• Natera will only contact candidates via email from an @natera.com domain. Be wary of fraudulent communications.
• Natera is an Equal Opportunity Employer committed to diversity and inclusion.