Vice President – Clinical and Medical Affairs

This is a fully remote position, open to applicants in North Carolina, +1 more state.

📋 Description

• Lead the operations of clinical studies, including evidence generation and the engagement and education of providers.

• Supervise the clinical operations team responsible for all clinical trials and partnerships.

• Direct the evidence generation team focused on the development, publication, and dissemination of clinical evidence.

• Collaborate with stakeholders to educate physicians, surgeons, and payors about NavDx testing.

• Develop multi-year roadmaps for evidence generation.

• Implement necessary studies, including both prospective and real-world evidence research.

• Guide the development of clinical strategies and plans for integrating technology into standard care protocols.

• Lead a cross-functional team to execute clinical project plans and convey program information.

• Act as a resource for peer-to-peer education on Naveris technologies.

• Take part in physician consultations and create educational materials.

• Collaborate with thought leaders on clinical practice guidelines.

• Represent Naveris at scientific and medical conferences as well as regulatory agencies.

• Ensure alignment with the Medical Laboratory Director for physician outreach and consultations.

• Provide executive leadership to the Clinical and Medical Affairs organization concerning personnel and budget issues.

⛳️ Requirements

• M.D., D.O., or M.D./Ph.D. with a valid license to practice medicine in the United States (required).

• Strongly preferred to be eligible for valid medical licenses in Massachusetts and North Carolina.

• Board Certification in Pathology, Medical Oncology, Radiation Oncology, Otolaryngology, Gynecologic Oncology, or Colorectal Surgery is strongly preferred.

• A minimum of 10 years of experience in direct patient care (including training and fellowship) concentrated in oncology.

• Proven history of scientific and clinical publications in prestigious journals.

• Demonstrated experience managing retrospective studies, including medical records and real-world data analysis.

• Comprehensive understanding of clinical research concepts, practices, and GCP and ICH Guidelines.

• Preferred industry experience, particularly in molecular diagnostics, liquid biopsy, or other oncology-related fields.

• Advantageous experience working with Medicare, commercial insurance, and other stakeholders in market access and the payor community.

• Experience with high-complexity CLIA laboratories for genomic testing technologies will set candidates apart.

🏝️ Benefits

• N/A