Sr Clinical Trial Manager, Oncology

Boston Scientific Gruppe; Hemel Hempstead; Remote; GBP 65,000 - 85,000; Full time

Job summary

A global medical technology company in Hemel Hempstead is seeking a Sr. Clinical Trial Manager to lead interventional oncology trials. This role involves strategic planning, global trial management, and collaboration with key stakeholders. The ideal candidate has over 5 years of oncology experience and proven trial management skills. The role is remote with some travel required.

Qualifications

• 5+ years of oncology-related experience.
• 1–3 years in early feasibility oncology clinical research.
• 1–3 years of project/trial management experience.
• Experience working with CROs and clinical vendors.

Responsibilities

• Lead strategic and operational planning of interventional oncology trials.
• Manage global clinical studies in alignment with strategy and budget.
• Collaborate on development of study materials and regulatory submissions.
• Present study progress and data to leadership.

Skills

Oncology-related experience

Project/trial management

Financial and budget management

Collaboration with CROs

Education

Bachelor’s degree

Job description

At Boston Scientific, we’re 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
• 1–3 years in early feasibility oncology clinical research
• 1–3 years of project/trial management experience
• 1–3 years of financial and budget management experience
• Experience working with CROs and clinical vendors

Preferred Qualifications

• Experience in sold tumor, medical device, or drug development
• Familiarity with product development teams
• Innovative thinking and problem-solving
• Strategic execution with minimal supervision
• Strong collaboration and influence across global stakeholders
• Adaptability in dynamic and uncertain environments

We are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate.

If you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply.