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Summit Therapeutics, Inc.

Senior Medical Director

Summit Therapeutics, Inc.

Senior Medical Director overseeing global Phase 3 clinical trials and BLA filings at Summit Therapeutics. Responsible for protocol design, medical oversight, and scientific advisory input.

Posted 7/8/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $253,000 - $317,000 per yearWebsite

About the role

Key responsibilities & impact
  • We are seeking a physician to serve as a Senior Medical Director to oversee global Phase 3 clinical trials and BLA (Biologic Licensing Application) filings.
  • The incumbent will be primarily responsible for developing and executing an integrated clinical trial programs including protocol design and medical oversight of new or ongoing studies.
  • They will be responsible for obtaining scientific advisory input, work with biostatisticians for phase 3 design and analyses, support regulatory interactions for product advancement, and work closely with clinical operations to provide advice and decision making regarding medical input to achieve operational excellence.
  • This position will provide medical insight across a myriad of functions from discovery to manufacturing are expected.
  • Additionally, the Medical Director will play a pivotal role in leading investigator engagements including travel to support face-to-face interaction and protocol training.
  • Prior experience in a mid-sized, fast-growing pharmaceutical environment is preferred, as this role will be working on product development in an extremely fast-paced and intense environment.
  • The Medical Director will serve as a leader on one multiple potentially pivotal programs.

Requirements

What you’ll need
  • 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/oncology
  • Working knowledge of clinical development pathways for hematology/oncology therapeutics in the US and EMA
  • Self-starter who will move forward with key initiatives without being prompted, able to perform a myriad of tasks needed to support the clinical development program, possesses a highly entrepreneurial and growth mindset, works collaboratively with cross-functional teams, loves a good mission.

Benefits

Comp & perks
  • Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location.
  • This may be different in other locations due to differences in the cost of labor.
  • The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.

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Hard Skills & Tools
Clinical Trial Program DevelopmentProtocol DesignMedical OversightBiostatistics CollaborationData Analysis
Soft Skills
Self-StarterEntrepreneurial MindsetCollaborative Work StyleMission-Driven
Certifications
Board Certification in Medicine