肿瘤学医学总监 (泌尿生殖聚焦)
Medical Director, Oncology (Genitourinary Focus)
医学主任,泌尿生殖系肿瘤负责推动临床开发、制定医疗策略、参与基础临床证据的生成,并与外部利益相关者合作,支持Natera在泌尿生殖系癌症(如前列腺、膀胱、肾脏及其他泌尿生殖系统恶性肿瘤)中的分子诊断。该职位在高级医学主任的监督下,将促进对癌症生物学的深入理解,同时推动变革性诊断技术在常规临床实践中的应用。
该职位适合一位在泌尿生殖系肿瘤领域具有专业技能和兴趣的放射肿瘤科医生,其热衷于将前沿分子诊断技术转化为临床实践,并在大规模范围内塑造精准肿瘤学的未来。
主要职责:
- 与泌尿生殖系肿瘤高级医学主任合作,制定并执行支持Natera在泌尿生殖系肿瘤中分子诊断工具(包括微小残留病(MRD)和ctDNA监测)的临床策略。
- 领导设计和实施整合Natera技术到标准泌尿生殖系肿瘤护理中的临床研究和治疗方案。
- 招募并联系泌尿生殖系肿瘤领域的领先主要研究者(PI)和临床研究中心参与公司资助的研究;与临床试验运营团队协作管理研究时间表和预算。
- 参与泌尿生殖系肿瘤产品组合的产品开发,识别临床未满足的需求、新产品机会、关键产品功能、预期用途、检测报告内容及最低验证要求。
- 提供上市后的医学事务支持,包括检测结果的解读、对医疗保健提供者的临床咨询以及患者咨询(检测前后)的指导。
- 作为泌尿生殖系肿瘤专家,为战略客户、区域销售和市场负责人、商业或临床领导所确定的重要合作和活动提供支持。
- 领导医学教育计划,包括外部培训、发布规划,以及针对泌尿生殖系恶性肿瘤的科学和临床材料的创建。
- 识别并招募泌尿生殖系肿瘤领域的关键意见领袖(KOL),担任顾问委员会成员并参与战略规划。
- 通过与科学传播团队合作,支持出版策略,撰写论文、摘要和会议报告。
查看英文原文
The Medical Director, Genitourinary Oncology is a critical leadership role responsible for advancing clinical development, shaping medical strategy, contributing to foundational clinical evidence generation, and engaging external stakeholders in support of Natera’s molecular diagnostics in GU cancers (e.g., prostate, bladder, kidney, and other genitourinary malignancies). This individual, under the oversight of a Senior Medical Director, will contribute to an evolving understanding of cancer biology while driving the adoption of transformational diagnostics into routine clinical practice.
This role is ideal for a radiation oncologist with specialized expertise and interest in GU cancers who is excited to translate cutting-edge molecular diagnostics into clinical practice and shape the future of precision oncology at scale.
Primary Responsibilities:
- Partner with the Senior Medical Director, Genitourinary Oncology to develop and execute clinical strategies supporting Natera’s molecular diagnostic tools for GU cancers, including minimal residual disease (MRD) and ctDNA-based monitoring.
- Lead the design and implementation of clinical studies and treatment protocols that integrate Natera’s technology into standard GU oncology care.
- Recruit and engage leading principal investigators (PIs) and clinical sites in GU oncology to participate in company-sponsored studies; manage study timelines and budgets in collaboration with Clinical Trial Operations.
- Advise on product development for the GU oncology portfolio, identifying clinical unmet needs, new product opportunities, key product features, intended use, test report content, and minimum validation requirements.
- Provide post-launch medical affairs support, including interpretation of test results, clinical consultation for healthcare providers, and guidance on patient counseling (pre- and post-test).
- Serve as GU oncology expert for support of high-value engagement and events identified by Strategic Accounts, Area Sales and Marketing leaders, commercial or clinical leadership.
- Lead medical education initiatives, including external training, launch planning, and the creation of scientific and clinical materials specific to GU malignancies.
- Identify and recruit Key Opinion Leaders (KOLs) in GU oncology to serve on advisory boards and contribute to strategic planning.
- Support the publication strategy by collaborating with Scientific Communications on manuscripts, abstracts, and conference presentations in GU oncology.
- Contribute to regulatory strategy by providing medical input into submissions related to GU cancer diagnostic products.
- Represent Natera’s medical voice externally through public relations, industry panels, advisory boards, and medical conferences, with a focus on GU oncology.
Qualifications:
- M.D. required (board-certified or board-eligible in Radiation Oncology preferred)
- Residency training in Radiation Oncology
- At least 3 years of post-residency clinical experience in GU cancers (prostate, bladder, kidney, etc.) as a primary treating radiation oncologist
- Deep knowledge of treatment paradigms, clinical guidelines, and diagnostic workflows in GU cancers
- Minimum 3 years of clinical trial experience in academic, biotech, or pharmaceutical settings
- Willingness to travel 40% (primarily U.S.-based, with occasional international travel)
Knowledge, Skills, and Abilities:
- Expertise in clinical trial design, regulatory/compliance frameworks, and biostatistics
- Strong understanding of evolving treatment landscapes in GU cancers (including targeted therapies, immunotherapy, and biomarker-driven approaches)
- Excellent analytical skills and scientific communication ability across varied audiences
- Quick learner with the ability to critically assess Natera’s technology and competing platforms
- Strong project management skills; comfortable balancing multiple complex initiatives
- Proven ability to lead and collaborate across cross-functional teams
- Skilled communicator, persuasive in scientific discussions and presentations
- Patient-focused and passionate about improving outcomes in GU cancers
- Capable of navigating complex systems and influencing without direct authority
Preferred Qualifications:
- Experience with ctDNA, MRD, or liquid biopsy technologies
- Established relationships with GU oncology KOLs and academic networks
- Experience supporting product launches or diagnostic adoption in oncology
#LI-TR1
Compensation & Total Rewards
This range reflects a good-faith estimate of the base pay we reasonably expect to offer at the time of hire. Final compensation will vary based on experience, qualifications, and internal equity considerations.
This position is also eligible for additional compensation and benefits through Natera’s robust Total Rewards program, including:
- 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
Compensation Range
$243,800—$304,700 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit www.natera.com.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
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Link: https://www.natera.com/notice-of-data-collection-california-residents/
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