Tech Stack

Description

As a key member of the Translational Medicine team, you will lead precision medicine and companion diagnostic (CDx) development for RAS(ON) inhibitors across solid cancers. You will drive CDx strategies from early to late-stage development, collaborate cross-functionally with diagnostic partners and internal teams, and manage analytical/clinical validation studies to support global regulatory submissions and launch readiness.

Requirements

• PhD with 6+ years or MS with 10+ years of relevant industry experience in biomarker or diagnostics
• 3+ years of experience in CDx development
• Expertise in in vitro diagnostic assay development (e.g., NGS, PCR, IHC)
• Subject matter expert in diagnostic regulation and global health authority interactions
• Excellent communication, collaboration, and planning skills

Responsibilities

• Drive CDx strategies to support early and late-stage development through registration and launch
• Lead joint project teams with diagnostic partners to execute analytical and clinical validation studies
• Collaborate with biomarker, clinical, and operations teams for sample collection and CDx testing
• Manage contracts, budgets, and timelines for CDx development milestones
• Develop patient identification strategies with commercial colleagues for launch readiness