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Role Overview:

  • Accountable for all aspects of clinical trial management for global studies, from start-up through close-out.
  • Lead and drive deliverables for assigned sites, countries, or regions across multiple studies or programs.

Key Responsibilities:

  • Oversee site selection, feasibility, activation, enrollment, monitoring, and closeout activities.
  • Partner with CROs to ensure robust trial execution, data monitoring, and patient enrollment strategies.
  • Draft and review study plans, informed consent forms, investigator agreements, and monitoring plans.

Experience and Skills:

  • Bachelor's degree in life science or related field preferred; 6+ years of clinical trial management experience.
  • 5+ years of direct CTM oversight, including Phase II/III trials; global oncology experience preferred.
  • Strong understanding of drug development, ICH guidelines, and GCP; excellent planning and communication skills.

Additional Information:

  • Ability to travel internationally up to 20% for site visits and study meetings.
  • Pay transparency: $122,000 - $145,000 USD per year, plus bonus, stock, and benefits.
  • Equal Opportunity Employer committed to a diverse and inclusive workplace.

Summit Therapeutics Inc.

Summit Therapeutics is a biopharmaceutical oncology company focused on improving quality of life and resolving unmet medical needs through innovative clinical studies. With multiple global Phase 3 trials and offices across the US, UK, and Ireland, the company is committed to a collaborative, people-driven culture.

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