Vice President, Clinical Development (Oncology & Molecular Diagnostics)

📋 Description

• Portfolio governance: monitor study health, enrollment, milestones, data readiness.
• Clinical utility design: lead cross-functional trials; define validity endpoints.
• Regulatory & CDx alignment: partner with Regulatory for FDA pathways and CDx strategy.
• Operational study health: manage internal operations and CROs to remove bottlenecks.
• Scientific footprint: publish and present at major oncology/diagnostic symposia.

🎯 Requirements

• MD, MD/PhD, or PhD with oncology pivotal trial leadership.
• 18+ years in clinical development; 10+ years directing oncology trials.
• Diagnostics-native fluency: cfDNA, ctDNA, MRD; validity concepts.
• Cross-functional leadership in matrixed environments with portfolio ownership.
• Proven strategies influencing regulatory submissions, registries, or LCDs.
• Bias for action; comfortable with ambiguity and critical portfolio trade-offs.

🎁 Benefits

• Medical, dental, vision, life and disability plans.
• Fertility care benefits and free testing for employees and families.
• Pregnancy/baby leave; 401k and commuter benefits.
• Employee referral program.