Senior Medical Director

Responsibilities

• Oversee global Phase 3 clinical trials and BLA filings
• Develop and execute integrated clinical trial programs including protocol design
• Provide medical oversight for new and ongoing studies
• Work cross-functionally with Medical Affairs, Regulatory, Commercial, and Clinical Operations
• Lead teams to execute clinical development goals and medical affairs planning
• Contribute to communication strategies via publications, manuscripts, and scientific presentations
• Direct human clinical trials (Phases 1-3) and ensure enrollment goals are met
• Participate in medical review of adverse event reports and safety data
• Coordinate information for reports submitted to FDA, EMA, and PMDA
• Present to external stakeholders including regulators and principal investigators

Requirements

• Board certified or eligible MD with hematology/oncology expertise
• 5+ years of experience in pharmaceutical, biologics, or biotech R&D
• Experience in clinical development stages for hematology/oncology
• Working knowledge of US and EMA clinical development pathways
• Strong collaborative and entrepreneurial mindset

About the Company

Summit Therapeutics Inc. is a biopharmaceutical oncology company focused on improving quality of life and resolving serious unmet medical needs through clinical studies in oncology.