Senior Clinical Trial Manager, Oncology

Boston Scientific•Marlborough, MA

34d•$127,900 - $243,000•Hybrid

About The Position

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. This 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.

Requirements

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

Nice To Haves

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

Responsibilities

Leading and driving the cross-functional project team in the planning, execution, and operational management of oncology clinical trials
Designing, directing, and executing global clinical studies in alignment with program strategy, approved budget, and timelines, in compliance with regulatory and operational procedures
Collaborating on development and oversight of internal and external project materials, including study manuals, systems, and regulatory submissions
Interfacing and building relationships with external physicians and key opinion leaders (KOLs)
Managing clinical trial budgets (up to 25%), including monthly tracking, forecasting, and variance analysis
Providing direction to Contract Research Organizations (CROs) and external vendors
Ensuring audit readiness and compliance across all clinical trial activities
Leading proactive risk identification, assessment, and mitigation planning for assigned studies
Preparing and delivering study updates, presentations, and risk assessments to leadership
Contributing clinical insights to product development activities and serving as a Clinical team representative on product development teams
Traveling domestically up to 10-25%, as required