Clinical Program Director – Precision Oncology Diagnostics, MRD Focus

Design, execute, and scale clinical development programs for precision oncology diagnostics. Ensure alignment with real‑world clinical decision‑making and guideline development. Define diagnostic‑focused study priorities and oversee study execution. Serve as a subject matter expert and lead working groups for oncology studies. Establish external partnerships for high‑quality study execution. Lead scientific communication and evidence dissemination. Support regulatory strategy and compliance.

Requirements

• Master’s degree in Certified Genetic Counseling
• 5 or more years of clinical experience in academia or oncology industry
• 3 or more years of experience in clinical development, clinical utility studies, and/or real‑world evidence generation.

Core Competencies

Demonstrates expertise in designing and executing clinical development programs for precision oncology diagnostics, with a strong focus on regulatory strategy and compliance. Proven ability to lead scientific communication and establish partnerships for high‑quality study execution.

Certifications & Qualifications

• Master’s Degree in Certified Genetic Counseling