Senior Clinical Trial Manager, Oncology

Additional Locations

US-MA-Marlborough; US-MN-Maple Grove

At Boston Scientific, we give you the opportunity to harness all that’s within you by working in teams of diverse, high‑performing employees tackling some of the most important health industry challenges. With access to the latest tools, information and training, we help you advance your skills and career and support your progress—whatever your ambitions.

As a Clinical Trial Manager, Oncology
, you will play a key leadership role within the Interventional Oncology & Embolization (IO&E) team, driving the design and execution of cutting‑edge oncology clinical trials. The position is responsible for leading cross‑functional teams on Early Feasibility Studies (EFS) and Phase II–III pivotal trials, with a strong focus on agility, innovation, and learning to advance Boston Scientific’s oncology pipeline. You will help shape the future of cancer care by enabling access to novel therapies and breakthrough technologies.

Boston Scientific values collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.

• Lead and drive the cross‑functional project team in the planning, execution, and operational management of oncology clinical trials
• Design, direct, and execute global clinical studies in alignment with program strategy, approved budget, and timelines, in compliance with regulatory and operational procedures
• Collaborate on development and oversight of internal and external project materials, including study manuals, systems, and regulatory submissions
• Interface and build relationships with external physicians and key opinion leaders (KOLs)
• Manage clinical trial budgets (up to 25%), including monthly tracking, forecasting, and variance analysis
• Provide direction to Contract Research Organizations (CROs) and external vendors
• Ensure audit readiness and compliance across all clinical trial activities
• Lead proactive risk identification, assessment, and mitigation planning for assigned studies
• Prepare and deliver study updates, presentations, and risk assessments to leadership
• Contribute clinical insights to product development activities and serve as a clinical team representative on product development teams
• Travel domestically up to 10‑25%, as required

• Bachelor’s degree and minimum of 5 years’ experience in oncology‑related clinical research or equivalent education and work experience
• Minimum of 1 year of direct oncology clinical trial management experience
• Minimum of 1 year of financial oversight and budget management experience
• Minimum of 1 year working with CROs, vendors, or outsourced clinical operations

• Experience in early feasibility studies, solid tumor trials, or immuno‑oncology (IO) product development
• Background working with engineering or product development teams
• Strong ability to:
  • Generate new ideas and approaches by applying creative thinking to complex problems
  • Align execution with strategic goals and independently drive action without close supervision
  • Collaborate and influence across global, cross‑functional teams
  • Adapt quickly and stay effective under changing conditions

Boston Scientific Corporation is an equal opportunity employer. All employment decisions are made without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity or expression, veteran status, age, disability, or any other protected class.