Oncology SVP Late Clinical Development

Job Summary

Reporting to the Chief Medical Officer, the full-time salaried Oncology SVP Late Clinical Development will provide medical leadership for late-stage clinical trials, oversee clinical development strategy, and collaborate across the portfolio, with the option to work remotely or from San Diego, CA.

Key responsibilities

• Lead the late clinical development function, including strategy, protocol development, and interactions with key opinion leaders
• Design and implement registration enabling clinical trials, ensuring integrity and communication of safety and efficacy data
• Contribute to regulatory filings and author clinical sections for NDAs and other documents while maintaining relationships with stakeholders

Required qualifications

• M.D. degree or equivalent with board certification in Oncology or Oncology/Hematology
• 12+ years of oncology clinical trial and drug development experience in the pharmaceutical or biotechnology industry
• Experience leading clinical aspects of regulatory filings and direct interaction with health authorities
• Proven executive leadership skills and ability to collaborate in a matrixed team environment
• Extensive knowledge of clinical trial methodology and regulatory compliance requirements