Description

You will lead the clinical development strategy for multiple oncology molecules, overseeing trial design, execution, and regulatory interactions. Your work will drive the development of novel RAS-targeted therapies from early-stage through commercialization.

Requirements

• MD, PhD, or advanced biomedical degree with 13+ years in pharma/biotech or academia (Associate Professor or higher)
• Extensive experience in data analysis and clinical relevance in pharma/biotech
• Proven track record designing and conducting multiple clinical trials from early to late stage, including Phase 1
• Experience authoring clinical development strategies and presenting for governance
• In-depth understanding of GCP, ICH, FDA, EMA regulations and leading Health Authority interactions

Responsibilities

• Develop and execute clinical development plans for multiple molecules
• Lead, mentor, and manage a cross-functional clinical development team
• Oversee clinical trial design, site selection, patient recruitment, data management, and regulatory compliance
• Establish relationships with investigators, regulatory agencies, and stakeholders
• Analyze clinical data to inform strategic decisions and guide program development