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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.