Senior Medical Director

The role

The Senior Medical Director will oversee global Phase 3 clinical trials and BLA filings. This person will develop and execute integrated clinical trial programs including protocol design and medical oversight.

What you will do

• Develop and execute integrated clinical trial programs including protocol design and medical oversight
• Obtain scientific advisory input
• Work with biostatisticians for phase 3 design and analyses
• Support regulatory interactions for product advancement
• Work with clinical operations to provide medical input
• Lead investigator engagements including travel for face-to-face interaction and protocol training
• Work cross functionally to develop overall product strategy
• Lead teams to execute on clinical development goals
• Manage direct reports or cross functional team members
• Contribute to communication strategy via publications, manuscripts, abstracts, posters and scientific presentations

Required qualifications

• Board certified or eligible MD with hematology/oncology product development and experience across stages of clinical development
• Minimum of 5+ years’ experience in pharmaceutical, biologics, or biotech R&D environment, or in a research environment involving the collection and analysis of human data in the area of hematology/onc
• Working knowledge of clinical development pathways for hematology/oncology therapeutics in the US and EMA
• Significant Oncology Experience

Nice to have

• Prior experience in a mid-sized, fast-growing pharmaceutical environment

Benefits

• bonus
• stock
• benefits

About the company

Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs.