Sr Clinical Trial Manager, Oncology

At Boston Scientific we are committed to transforming lives through less invasive products and technologies that diagnose and treat a wide range of medical conditions. Our innovations span key therapeutic areas and are expanding into new geographies and high-growth adjacent markets.

Our Interventional Oncology and Embolization (IO&E) portfolio empowers physicians to treat tumors less invasively. It includes:

• Embolization technologies
• TheraSphere Y90 transarterial radioembolization
• Ablation technologies

All designed to prevent tumor growth and induce necrosis, helping physicians save lives and limbs around the world.

About the Role: Sr. Clinical Trial Manager Oncology

As a Sr. Clinical Trial Manager you will lead cross‑functional teams in the execution of Early Feasibility Studies (EFS) in oncology. This role emphasizes agility, learning and creative problem‑solving to accelerate the development of breakthrough cancer therapies.

The role is remote with 10‑25% travel required and can be based in any of our EMEA locations.

Key Responsibilities

• Lead strategic and operational planning of interventional oncology trials
• Manage global clinical studies in alignment with strategy, budget and SOPs
• Collaborate on development of study materials, systems and regulatory submissions
• Engage with external physicians and key opinion leaders (KOLs)
• Oversee clinical trial budgets (up to 25%) including forecasting and variance reviews
• Direct CROs and clinical vendors
• Ensure audit readiness and risk management throughout the study lifecycle
• Present study progress data and risks to leadership
• Provide clinical input to product development teams
• Domestic travel: 10‑25%

Required Qualifications

• Bachelor’s degree with 5 years of oncology‑related experience
• 13 years in early feasibility oncology clinical research
• 13 years of project / trial management experience
• 13 years of financial and budget management experience
• Experience working with CROs and clinical vendors

Preferred Qualifications

• Experience in solid tumor medical device or drug development
• Familiarity with product development teams

Key Competencies

• Innovative thinking and problem‑solving
• Strategic execution with minimal supervision
• Strong collaboration and influence across global stakeholders
• Adaptability in dynamic and uncertain environments