Associate Medical Director - Gynecologic Cancer

Shape the future of cancer care as an Associate Medical Director, Oncology at Natera. In this strategic leadership role, you will provide medical expertise for Natera's oncology portfolio, collaborating with cross-functional teams across research, development, commercial, and medical affairs. You will ensure the scientific integrity and clinical adoption of our oncology testing solutions. Primary Responsibilities: - Clinical Development: - Collaborate with the Sr. Medical Director, Oncology on the clinical development of ctDNA-based diagnostics. - Lead development and implementation of clinical strategies for Natera's oncology products. - Medical Education and Communication: - Oversee medical education and scientific communication for healthcare providers on Natera's oncology offerings. - Partner with the commercial team to develop and deliver compelling medical messages for Natera's oncology products. - Representation and Advocacy: - Represent Natera at medical conferences and industry events, in person and virtual. - Foster a culture of scientific excellence and intellectual curiosity within the oncology team. - Research and Development: - Collaborate with research and development teams on clinical trial design, data analysis, and publication. Key Skill Sets / Responsibilities: - Endometrium cancer-Specific Expertise is ideal: - Strong knowledge in Gynecologic Cancer, with the ability to develop and implement strategies specific to Gynecologic oncology. - Provide expert guidance and support on Gynecologic oncology cases and clinical trials. - Comprehensive Oncology Knowledge: - Ability to speak to all histologies and indications, ensuring broad expertise across the oncology spectrum. - Stay updated on the latest advancements in various cancer types and integrate this knowledge into Natera’s oncology products. - Cross-Disciplinary Collaboration: - Work effectively with cross-functional teams including research, development, commercial, and medical affairs to drive the success of oncology initiatives. - Coordinate with internal and external stakeholders to ensure the clinical relevance and adoption of Natera’s oncology solutions. Qualifications: - M.D. or D.O. degree with board certification in Oncology required. - At least 5 years of experience in oncology, with a strong background in clinical research and development. Strong knowledge in endometrium cancer preferred. - At least 3 years of clinical trial experience in academia, biotech industry, or equivalent. - Associate/full medical director designation commensurate with experience. Knowledge, Skills, and Abilities: - Ability to quickly learn Natera’s technology and that of our competitors, understanding the strengths and limitations of each, and articulate strong customer value propositions. - Proven skill and experience in building and managing a team. - Effective written and oral communication skills, with strong persuasive abilities and quick thinking. - Project management skills, with the ability to balance and execute multiple projects simultaneously. - Proven team player, capable of participating as a member of a cross-disciplinary team. - Ability to manage conflict with poise. - Strong knowledge of clinical trial methodology, protocol development, regulatory and compliance requirements, statistics, and epidemiology is preferred. Physical Demands & Work Environment: - Duties are typically performed in an office setting. - This position requires the ability to use a computer keyboard, communicate over the telephone, and read printed material. - Duties may occasionally require working outside normal working hours (evenings and weekends).