Caitlin Schonewolf: Hiring Medical Director to Lead Skin and Immuno-Oncology at Natera

About the role

Natera is seeking a Medical Director to lead Skin and Immuno-Oncology. The role will shape the science, strategy, and clinical adoption of Signatera, a ctDNA-based solution that informs care in cutaneous malignancies and immunotherapy-treated solid tumors. The Medical Director will work closely with key opinion leaders and cross-functional leaders to drive evidence generation and integrate Signatera into standard oncology practice.

Responsibilities

• Lead the development and execution of clinical strategies for skin and immuno-oncology applications of Natera’s ctDNA-based solutions.
• Collaborate with key opinion leaders and cross-functional teams to advance the understanding and acceptance of Signatera in the medical community.
• Develop and maintain strong relationships with healthcare providers, payers, and other stakeholders to ensure the successful adoption of Signatera.
• Contribute to the scientific literature and industry guidelines to establish best practices for the use of ctDNA in oncology.
• Support the commercialization efforts of Natera’s products by providing expert guidance and insights.

Requirements

• A MD or DO degree with board certification in internal medicine or an equivalent specialty.
• At least 10 years of relevant experience in oncology, dermatology, or related fields.
• Experience in leading clinical research and translational science projects.
• Strong track record of influencing clinical practice and translating scientific discoveries into real-world impact.
• Excellent communication and collaboration skills, with the ability to work effectively with diverse stakeholders.

Qualifications

• PhD in a relevant field (e.g., molecular biology, bioinformatics) with a minimum of 5 years of experience in oncology research.
• Proven ability to generate and publish high-quality research papers in peer-reviewed journals.
• Experience in developing and managing large-scale clinical trials.
• Knowledge of regulatory requirements and industry standards for clinical research.

Skills

• Expertise in ctDNA analysis and its application in oncology.
• Strong leadership and project management skills.
• Ability to communicate complex scientific concepts to non-scientific audiences.
• Experience in building and maintaining strategic partnerships with academic institutions and industry partners.

Benefits

• Competitive salary and benefits package.
• Flexible work schedule to support work-life balance.
• Opportunities for professional growth and advancement within the company.
• Access to cutting-edge technology and resources in the field of oncology.

Pay

Commensurate with experience.

Schedule

Full-time.

Note: The exact details for Pay and Schedule may vary based on the candidate's qualifications and experience.