• MD plus accredited fellowship in Pathology
• Strong foundation in Life Sciences e.g. Molecular Biology, Pathology
• Experience with clinical companion diagnostic development
• 5+ years Medical Affairs experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO) that includes collaborations with integrated delivery networks, accountable care organizations, and/or payers
• Experience with stakeholder engagement and interactions (e.g., OLs, advocacy groups, payers)
• Familiarity with global regulatory organizations, guidelines, and practices
• Knowledge of Good Clinical Practices (GCP) and global regulations and guidelines
• Knowledge of pharmaceutical product development, product life cycle, and commercialization processes, including but not limited to, clinical operations, commercial, regulatory, and medical affairs specifically related to companion diagnostics
• History of solving problems while exhibiting sound scientific/medical judgment and a balanced, realistic understanding of issues
• In-depth understanding of scientific method and clinical applications based on medical, scientific, and practical rationale
• Track record of success collaborating in matrix-ed cross-functional teams
• Outstanding written and verbal communication skills